Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221937 |
| ensemblid | ENSG00000164916.11 |
| hgncid | 23480 |
| symbol | FOXK1 |
| name | forkhead box K1 |
| refseq_nuc | NM_001037165.2 |
| refseq_prot | NP_001032242.1 |
| ensembl_nuc | ENST00000328914.5 |
| ensembl_prot | ENSP00000328720.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 4682295 |
| end | 4771442 |
| strand | + |
| ver | v1.2 |
| region | chr7:4682295-4771442 |
| region5000 | chr7:4677295-4776442 |
| regionname0 | FOXK1_chr7_4682295_4771442 |
| regionname5000 | FOXK1_chr7_4677295_4776442 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 733 | 283 | 89 | 50 | 95 | 9 | 38 | 58 | FOXK1_chr7_4677295_4776442 | FOXK1 | MAEVG others(728): Show |
chr7 | 4677295 | 4776442 |
| a0002 | 0/0 | 733 | 5 | 3 | 1 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | MAEVG others(728): Show |
chr7 | 4677295 | 4776442 |
| a0003 | 0/0 | 733 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | MAEVG others(728): Show |
chr7 | 4677295 | 4776442 |
| a0004 | 0/0 | 733 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | MAEVG others(728): Show |
chr7 | 4677295 | 4776442 |
| a0005 | 0/0 | 733 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | MAEVG others(728): Show |
chr7 | 4677295 | 4776442 |
| a0006 | 0/0 | 733 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | MAEVG others(728): Show |
chr7 | 4677295 | 4776442 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2199 | 103 | 7 | 15 | 61 | 3 | 16 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0002 | 0/0 | 2199 | 61 | 20 | 14 | 13 | 4 | 10 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0003 | 0/0 | 2199 | 50 | 41 | 4 | 2 | 0 | 3 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0004 | 0/0 | 2199 | 28 | 7 | 3 | 10 | 0 | 8 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0005 | 0/0 | 2199 | 7 | 1 | 5 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0006 | 0/0 | 2199 | 5 | 3 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0007 | 0/0 | 2199 | 5 | 5 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0008 | 0/0 | 2199 | 4 | 0 | 0 | 4 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0009 | 0/0 | 2199 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0010 | 1/0 | 2199 | 3 | 0 | 1 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0011 | 0/0 | 2199 | 3 | 1 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0015 | 0/0 | 2199 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0017 | 0/0 | 2199 | 2 | 0 | 1 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0019 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0021 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0022 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0023 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0024 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0026 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0001c0027 | 0/0 | 2199 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0002c0012 | 0/0 | 2199 | 2 | 1 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0002c0013 | 0/0 | 2199 | 2 | 1 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0002c0018 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0003c0014 | 0/0 | 2199 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0004c0016 | 0/0 | 2199 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0005c0025 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 | ||
| a0006c0020 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | ATGGC others(2194): Show |
chr7 | 4677295 | 4776442 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11194 | 72 | 3 | 11 | 43 | 2 | 13 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0006 | 0/0 | 11193 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0019 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10866): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0020 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0021 | 0/0 | 11191 | 2 | 0 | 1 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0022 | 0/0 | 11194 | 2 | 0 | 0 | 2 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0023 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0030 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0042 | 0/0 | 11193 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0043 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0047 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10866): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0048 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0049 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0051 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0052 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0053 | 0/1 | 11198 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11193): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0054 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0055 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0056 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0057 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0058 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0059 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0061 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0064 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0065 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0067 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0068 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0001t0077 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0001 | 0/0 | 11194 | 35 | 2 | 11 | 12 | 3 | 7 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0002 | 0/0 | 11193 | 11 | 11 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0006 | 0/0 | 11193 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0020 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0023 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0027 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0033 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10866): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0034 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0036 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0044 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0046 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0050 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0060 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0063 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0066 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0069 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0002t0074 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0001 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0002 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0003 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0005 | 0/0 | 11191 | 4 | 4 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0008 | 0/0 | 10871 | 4 | 4 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10866): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0011 | 0/0 | 11191 | 3 | 3 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0012 | 0/0 | 11193 | 3 | 3 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0015 | 0/0 | 11191 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0017 | 0/0 | 11194 | 3 | 0 | 2 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0018 | 0/0 | 11191 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0024 | 0/0 | 11191 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0025 | 0/0 | 10871 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10866): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0026 | 0/0 | 11194 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0031 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0032 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0039 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0062 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0070 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0071 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0072 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0073 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0080 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0081 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0082 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0083 | 0/0 | 11193 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0086 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0091 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0092 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0094 | 0/0 | 10874 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10869): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0095 | 0/0 | 11186 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11181): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0096 | 0/0 | 11189 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11184): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0098 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0003t0099 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0001 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0003 | 0/0 | 11193 | 4 | 0 | 0 | 3 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0005 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0007 | 0/0 | 11194 | 5 | 0 | 0 | 5 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0010 | 0/0 | 11193 | 4 | 0 | 0 | 0 | 0 | 4 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0011 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0028 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0029 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0035 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0038 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0040 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0045 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0084 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0085 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0088 | 0/0 | 11193 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0089 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0093 | 0/0 | 11193 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0004t0097 | 0/0 | 11188 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11183): Show |
chr7 | 4677295 | 4776442 |
| a0001c0005t0001 | 0/0 | 11194 | 4 | 0 | 4 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0005t0006 | 0/0 | 11193 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0005t0014 | 0/0 | 11194 | 2 | 1 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0006t0009 | 0/0 | 11193 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0006t0013 | 0/0 | 11193 | 3 | 3 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0007t0004 | 0/0 | 10874 | 4 | 4 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10869): Show |
chr7 | 4677295 | 4776442 |
| a0001c0007t0078 | 0/0 | 10874 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10869): Show |
chr7 | 4677295 | 4776442 |
| a0001c0008t0003 | 0/0 | 11193 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0008t0087 | 0/0 | 11193 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0009t0003 | 0/0 | 11193 | 3 | 0 | 0 | 3 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0010t0001 | 1/0 | 11194 | 2 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0010t0079 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0011t0004 | 0/0 | 10874 | 3 | 1 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10869): Show |
chr7 | 4677295 | 4776442 |
| a0001c0015t0009 | 0/0 | 11193 | 2 | 2 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0001c0017t0016 | 0/0 | 11194 | 2 | 0 | 1 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0019t0090 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0001c0021t0016 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0022t0001 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0023t0041 | 0/0 | 11194 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0024t0001 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0026t0001 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0001c0027t0001 | 0/0 | 11194 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0002c0012t0002 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0002c0012t0019 | 0/0 | 10871 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10866): Show |
chr7 | 4677295 | 4776442 |
| a0002c0013t0008 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(10866): Show |
chr7 | 4677295 | 4776442 |
| a0002c0013t0015 | 0/0 | 11191 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0002c0018t0005 | 0/0 | 11191 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11186): Show |
chr7 | 4677295 | 4776442 |
| a0003c0014t0001 | 0/0 | 11194 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0004c0016t0075 | 0/0 | 11216 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11211): Show |
chr7 | 4677295 | 4776442 |
| a0004c0016t0076 | 0/0 | 11193 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11188): Show |
chr7 | 4677295 | 4776442 |
| a0005c0025t0014 | 0/0 | 11194 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| a0006c0020t0037 | 0/0 | 11194 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | GGAGC others(11189): Show |
chr7 | 4677295 | 4776442 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0019g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0021g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0021g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0022g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0022g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0023g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0030g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0042g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0043g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0047g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0048g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0049g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0051g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0052g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0053g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0054g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0055g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0056g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0057g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0058g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0059g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0061g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0064g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0065g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0067g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0068g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0001t0077g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0020g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0023g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0027g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0033g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0034g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0036g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0044g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0046g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0050g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0060g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0063g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0066g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0069g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0002t0074g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0012g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0015g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0017g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0017g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0017g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0018g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0024g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0024g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0025g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0025g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0026g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0026g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0031g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0032g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0039g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0062g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0070g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0071g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0072g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0073g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0080g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0081g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0082g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0083g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0086g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0091g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0092g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0094g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0095g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0096g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0098g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0003t0099g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0010g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0010g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0010g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0028g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0029g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0035g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0038g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0040g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0045g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0084g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0085g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0088g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0089g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0093g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0004t0097g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0005t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0005t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0005t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0005t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0005t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0005t0014g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0006t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0006t0013g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0006t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0006t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0007t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0007t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0007t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0007t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0007t0078g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0008t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0008t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0008t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0008t0087g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0009t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0009t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0009t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0010t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0010t0001g0256 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0010t0079g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0011t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0011t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0011t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0015t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0015t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0017t0016g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0017t0016g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0019t0090g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0021t0016g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0022t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0023t0041g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0024t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0026t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0001c0027t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0002c0012t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0002c0012t0019g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0002c0013t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0002c0013t0015g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0002c0018t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0003c0014t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0003c0014t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0004c0016t0075g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0004c0016t0076g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0005c0025t0014g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| a0006c0020t0037g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0131 | EUR | GBR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0216 | EUR | FIN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00323 | hp2 | a0001 | c0027 | t0001 | g0217 | EUR | FIN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00408 | hp1 | a0001 | c0001 | t0048 | g0193 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00597 | hp1 | a0001 | c0008 | t0003 | g0264 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00621 | hp2 | a0005 | c0025 | t0014 | g0033 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0166 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00673 | hp2 | a0001 | c0001 | t0030 | g0065 | EAS | CHS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00738 | hp1 | a0001 | c0024 | t0001 | g0212 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG00738 | hp2 | a0001 | c0004 | t0029 | g0029 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0113 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01070 | hp2 | a0001 | c0006 | t0009 | g0002 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01071 | hp1 | a0001 | c0006 | t0009 | g0002 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01074 | hp1 | a0001 | c0003 | t0017 | g0157 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01074 | hp2 | a0003 | c0014 | t0001 | g0058 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01081 | hp1 | a0001 | c0003 | t0098 | g0174 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01081 | hp2 | a0001 | c0011 | t0004 | g0078 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0114 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01106 | hp2 | a0001 | c0001 | t0057 | g0019 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01109 | hp1 | a0002 | c0012 | t0019 | g0290 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01109 | hp2 | a0001 | c0010 | t0079 | g0273 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01175 | hp1 | a0001 | c0001 | t0042 | g0139 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01175 | hp2 | a0001 | c0001 | t0021 | g0023 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01192 | hp2 | a0001 | c0002 | t0023 | g0048 | AMR | PUR | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01258 | hp2 | a0001 | c0017 | t0016 | g0106 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01261 | hp1 | a0001 | c0021 | t0016 | g0270 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01346 | hp1 | a0001 | c0002 | t0034 | g0158 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01361 | hp1 | a0001 | c0003 | t0017 | g0173 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01496 | hp1 | a0001 | c0002 | t0046 | g0244 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01496 | hp2 | a0001 | c0011 | t0004 | g0280 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0051 | EUR | IBS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01515 | hp2 | a0001 | c0001 | t0021 | g0012 | EUR | IBS | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01884 | hp2 | a0001 | c0011 | t0004 | g0251 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01891 | hp1 | a0001 | c0001 | t0067 | g0094 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01891 | hp2 | a0001 | c0003 | t0081 | g0007 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01928 | hp1 | a0001 | c0001 | t0051 | g0025 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01934 | hp1 | a0003 | c0014 | t0001 | g0171 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01978 | hp1 | a0001 | c0004 | t0028 | g0028 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01978 | hp2 | a0001 | c0005 | t0001 | g0223 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01981 | hp1 | a0001 | c0005 | t0014 | g0169 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02004 | hp1 | a0001 | c0026 | t0001 | g0099 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02004 | hp2 | a0001 | c0005 | t0001 | g0154 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02055 | hp1 | a0001 | c0002 | t0033 | g0103 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02055 | hp2 | a0001 | c0003 | t0011 | g0284 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02056 | hp1 | a0001 | c0001 | t0049 | g0039 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0258 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02080 | hp2 | a0001 | c0001 | t0043 | g0053 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02132 | hp2 | a0001 | c0002 | t0006 | g0194 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02135 | hp2 | a0001 | c0001 | t0077 | g0123 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02145 | hp2 | a0001 | c0007 | t0004 | g0085 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02155 | hp1 | a0001 | c0001 | t0061 | g0183 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | CDX | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02257 | hp1 | a0001 | c0003 | t0012 | g0100 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0227 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02258 | hp2 | a0001 | c0004 | t0040 | g0186 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02273 | hp1 | a0001 | c0005 | t0001 | g0175 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02280 | hp1 | a0001 | c0003 | t0011 | g0081 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02280 | hp2 | a0002 | c0012 | t0002 | g0291 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02451 | hp1 | a0001 | c0003 | t0095 | g0073 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0243 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | KHV | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02572 | hp1 | a0001 | c0003 | t0011 | g0236 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02615 | hp1 | a0001 | c0006 | t0013 | g0077 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02615 | hp2 | a0001 | c0004 | t0011 | g0255 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0238 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02622 | hp2 | a0001 | c0003 | t0062 | g0072 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02630 | hp1 | a0001 | c0007 | t0004 | g0234 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0252 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02647 | hp1 | a0001 | c0003 | t0012 | g0229 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02647 | hp2 | a0001 | c0003 | t0015 | g0086 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02698 | hp1 | a0001 | c0001 | t0023 | g0015 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02698 | hp2 | a0001 | c0003 | t0092 | g0149 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02717 | hp1 | a0001 | c0003 | t0072 | g0208 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02717 | hp2 | a0001 | c0003 | t0008 | g0101 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02723 | hp1 | a0001 | c0001 | t0047 | g0249 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02723 | hp2 | a0001 | c0003 | t0008 | g0074 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02809 | hp1 | a0001 | c0003 | t0008 | g0262 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0226 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02818 | hp1 | a0001 | c0003 | t0080 | g0060 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02818 | hp2 | a0001 | c0003 | t0008 | g0197 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02895 | hp1 | a0001 | c0003 | t0018 | g0283 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02896 | hp1 | a0004 | c0016 | t0075 | g0150 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02896 | hp2 | a0001 | c0003 | t0024 | g0071 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02897 | hp1 | a0004 | c0016 | t0076 | g0151 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02922 | hp1 | a0001 | c0004 | t0045 | g0232 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02922 | hp2 | a0001 | c0003 | t0099 | g0176 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02965 | hp1 | a0001 | c0003 | t0096 | g0004 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0241 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02970 | hp1 | a0001 | c0003 | t0031 | g0005 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02970 | hp2 | a0001 | c0003 | t0070 | g0281 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02976 | hp1 | a0001 | c0003 | t0005 | g0242 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02976 | hp2 | a0001 | c0004 | t0035 | g0092 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03017 | hp1 | a0001 | c0001 | t0054 | g0129 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03041 | hp1 | a0001 | c0003 | t0018 | g0207 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03041 | hp2 | a0001 | c0002 | t0044 | g0087 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03098 | hp1 | a0001 | c0003 | t0094 | g0286 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03098 | hp2 | a0001 | c0003 | t0005 | g0247 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03130 | hp1 | a0001 | c0002 | t0069 | g0268 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03130 | hp2 | a0001 | c0006 | t0013 | g0075 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03139 | hp1 | a0001 | c0003 | t0073 | g0093 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03139 | hp2 | a0001 | c0003 | t0091 | g0278 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03209 | hp1 | a0001 | c0003 | t0071 | g0250 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03209 | hp2 | a0001 | c0007 | t0078 | g0090 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03225 | hp1 | a0001 | c0002 | t0063 | g0253 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03225 | hp2 | a0001 | c0003 | t0012 | g0067 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03239 | hp1 | a0001 | c0004 | t0084 | g0109 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03453 | hp1 | a0001 | c0019 | t0090 | g0219 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03453 | hp2 | a0001 | c0003 | t0015 | g0246 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03486 | hp2 | a0001 | c0004 | t0097 | g0248 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03491 | hp1 | a0001 | c0004 | t0010 | g0001 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03491 | hp2 | a0001 | c0003 | t0017 | g0143 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03492 | hp1 | a0001 | c0004 | t0010 | g0001 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03516 | hp1 | a0001 | c0007 | t0004 | g0089 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03516 | hp2 | a0002 | c0018 | t0005 | g0289 | AFR | ESN | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03540 | hp1 | a0001 | c0004 | t0005 | g0263 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03540 | hp2 | a0001 | c0002 | t0066 | g0209 | AFR | GWD | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03579 | hp1 | a0001 | c0003 | t0025 | g0210 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03579 | hp2 | a0001 | c0003 | t0024 | g0088 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03654 | hp1 | a0001 | c0004 | t0003 | g0032 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03669 | hp2 | a0001 | c0002 | t0050 | g0134 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0112 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03688 | hp2 | a0001 | c0003 | t0003 | g0199 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03704 | hp1 | a0001 | c0001 | t0056 | g0024 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03710 | hp1 | a0001 | c0004 | t0010 | g0182 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03710 | hp2 | a0001 | c0004 | t0085 | g0049 | SAS | PJL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03927 | hp1 | a0001 | c0017 | t0016 | g0122 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03927 | hp2 | a0001 | c0002 | t0036 | g0156 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04115 | hp1 | a0001 | c0004 | t0010 | g0137 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04184 | hp2 | a0001 | c0004 | t0093 | g0274 | SAS | BEB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04199 | hp2 | a0001 | c0002 | t0027 | g0018 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18522 | hp1 | a0001 | c0003 | t0026 | g0079 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18522 | hp2 | a0001 | c0002 | t0020 | g0285 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18747 | hp2 | a0001 | c0003 | t0083 | g0152 | EAS | CHB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0224 | AFR | YRI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18940 | hp2 | a0001 | c0004 | t0003 | g0228 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18942 | hp2 | a0001 | c0008 | t0003 | g0206 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18950 | hp1 | a0001 | c0001 | t0059 | g0231 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18950 | hp2 | a0001 | c0001 | t0065 | g0203 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18951 | hp2 | a0001 | c0004 | t0003 | g0140 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18954 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18959 | hp2 | a0001 | c0022 | t0001 | g0211 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18960 | hp1 | a0001 | c0005 | t0006 | g0167 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18962 | hp1 | a0001 | c0004 | t0089 | g0198 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18962 | hp2 | a0001 | c0004 | t0003 | g0120 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18964 | hp1 | a0001 | c0001 | t0055 | g0027 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18969 | hp2 | a0001 | c0009 | t0003 | g0165 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18980 | hp1 | a0001 | c0001 | t0022 | g0003 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18985 | hp1 | a0001 | c0008 | t0087 | g0271 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18995 | hp2 | a0001 | c0004 | t0007 | g0180 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA18999 | hp2 | a0001 | c0001 | t0068 | g0052 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19002 | hp1 | a0001 | c0001 | t0064 | g0045 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19002 | hp2 | a0001 | c0004 | t0007 | g0141 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19030 | hp1 | a0001 | c0004 | t0038 | g0010 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19043 | hp1 | a0001 | c0002 | t0074 | g0237 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19043 | hp2 | a0001 | c0007 | t0004 | g0084 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19056 | hp2 | a0001 | c0004 | t0007 | g0008 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19058 | hp1 | a0001 | c0004 | t0007 | g0233 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19058 | hp2 | a0001 | c0001 | t0052 | g0146 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19060 | hp1 | a0001 | c0001 | t0022 | g0220 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19060 | hp2 | a0001 | c0003 | t0086 | g0213 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19062 | hp1 | a0001 | c0004 | t0088 | g0272 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19066 | hp1 | a0001 | c0001 | t0058 | g0064 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19066 | hp2 | a0001 | c0009 | t0003 | g0142 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19070 | hp2 | a0001 | c0009 | t0003 | g0164 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19082 | hp2 | a0001 | c0004 | t0007 | g0144 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19085 | hp1 | a0001 | c0008 | t0003 | g0095 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20129 | hp1 | a0001 | c0015 | t0009 | g0225 | AFR | ASW | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ASW | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20752 | hp1 | a0001 | c0010 | t0001 | g0159 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20752 | hp2 | a0001 | c0002 | t0060 | g0104 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20805 | hp1 | a0002 | c0013 | t0015 | g0287 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | GIH | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG01123 | hp2 | a0006 | c0020 | t0037 | g0218 | AMR | CLM | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02109 | hp1 | a0001 | c0003 | t0039 | g0082 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02109 | hp2 | a0001 | c0003 | t0032 | g0083 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02486 | hp1 | a0001 | c0006 | t0013 | g0076 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02486 | hp2 | a0001 | c0023 | t0041 | g0105 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG02559 | hp2 | a0002 | c0013 | t0008 | g0288 | AFR | ACB | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03471 | hp1 | a0001 | c0003 | t0082 | g0275 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG03471 | hp2 | a0001 | c0015 | t0009 | g0279 | AFR | MSL | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20300 | hp1 | a0001 | c0005 | t0014 | g0168 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA20300 | hp2 | a0001 | c0003 | t0026 | g0080 | AFR | USA | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA21309 | hp1 | a0001 | c0003 | t0025 | g0254 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| NA21309 | hp2 | a0001 | c0003 | t0005 | g0091 | AFR | LWK | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0053 | g0011 | REF | REF | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| homoSapiens | grch38p0 | a0001 | c0010 | t0001 | g0256 | REF | REF | FOXK1_chr7_4677295_4776442 | FOXK1 | chr7 | 4677295 | 4776442 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4682510 | G | A | 1 | a0002 | 5 | HG01109.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
missense_variant | MODERATE | c.202G>A | p.Ala68Thr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/9 | 216/11194 | 202/2202 | 68/733 | chr7 | 4682510 | |||
| chr7:4759469 | A | G | 1 | a0005 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1570A>G | p.Met524Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/9 | 1584/11194 | 1570/2202 | 524/733 | chr7 | 4759469 | |||
| chr7:4761084 | A | G | 1 | a0004 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1717A>G | p.Ile573Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/9 | 1731/11194 | 1717/2202 | 573/733 | chr7 | 4761084 | |||
| chr7:4762301 | C | T | 1 | a0006 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2039C>T | p.Ala680Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2053/11194 | 2039/2202 | 680/733 | chr7 | 4762301 | |||
| chr7:4762342 | G | A | 1 | a0003 | 2 | HG01074.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.2080G>A | p.Ala694Thr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2094/11194 | 2080/2202 | 694/733 | chr7 | 4762342 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4682746 | G | A | 2 | a0001c0005 a0001c0009 |
10 | HG00639.hp2 HG01978.hp2 HG01981.hp1 others(7): Show |
synonymous_variant | LOW | c.438G>A | p.Arg146Arg | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/9 | 452/11194 | 438/2202 | 146/733 | chr7 | 4682746 | |||
| chr7:4740883 | G | T | 15 | a0001c0001 a0001c0004 a0001c0005 others(12): Show |
159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
synonymous_variant | LOW | c.606G>T | p.Thr202Thr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/9 | 620/11194 | 606/2202 | 202/733 | chr7 | 4740883 | |||
| chr7:4755263 | C | T | 1 | a0001c0027 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.930C>T | p.Tyr310Tyr | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/9 | 944/11194 | 930/2202 | 310/733 | chr7 | 4755263 | |||
| chr7:4759099 | C | T | 2 | a0001c0007 a0001c0011 |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
synonymous_variant | LOW | c.1293C>T | p.Ser431Ser | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/9 | 1307/11194 | 1293/2202 | 431/733 | chr7 | 4759099 | |||
| chr7:4759126 | G | A | 1 | a0001c0019 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1320G>A | p.Leu440Leu | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/9 | 1334/11194 | 1320/2202 | 440/733 | chr7 | 4759126 | |||
| chr7:4759144 | C | T | 1 | a0001c0026 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.1338C>T | p.Pro446Pro | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/9 | 1352/11194 | 1338/2202 | 446/733 | chr7 | 4759144 | |||
| chr7:4759504 | C | T | 1 | a0001c0024 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.1605C>T | p.Ala535Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/9 | 1619/11194 | 1605/2202 | 535/733 | chr7 | 4759504 | |||
| chr7:4759510 | A | T | 3 | a0001c0017 a0001c0021 a0001c0023 |
4 | HG01258.hp2 HG01261.hp1 HG02486.hp2 others(1): Show |
synonymous_variant | LOW | c.1611A>T | p.Gly537Gly | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/9 | 1625/11194 | 1611/2202 | 537/733 | chr7 | 4759510 | |||
| chr7:4761089 | G | A | 1 | a0001c0024 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.1722G>A | p.Ala574Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/9 | 1736/11194 | 1722/2202 | 574/733 | chr7 | 4761089 | |||
| chr7:4762194 | C | T | 3 | a0001c0006 a0001c0015 a0004c0016 |
9 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(6): Show |
synonymous_variant | LOW | c.1932C>T | p.Ser644Ser | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1946/11194 | 1932/2202 | 644/733 | chr7 | 4762194 | |||
| chr7:4762221 | G | A | 1 | a0005c0025 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1959G>A | p.Ala653Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1973/11194 | 1959/2202 | 653/733 | chr7 | 4762221 | |||
| chr7:4762293 | G | A | 1 | a0001c0022 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.2031G>A | p.Ala677Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2045/11194 | 2031/2202 | 677/733 | chr7 | 4762293 | |||
| chr7:4762398 | T | G | 26 | a0001c0001 a0001c0002 a0001c0003 others(23): Show |
290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
synonymous_variant | LOW | c.2136T>G | p.Gly712Gly | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2150/11194 | 2136/2202 | 712/733 | chr7 | 4762398 | |||
| chr7:4762401 | T | C | 1 | a0001c0008 | 4 | HG00597.hp1 NA18942.hp2 NA18985.hp1 others(1): Show |
synonymous_variant | LOW | c.2139T>C | p.Ala713Ala | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2153/11194 | 2139/2202 | 713/733 | chr7 | 4762401 | |||
| chr7:4762404 | A | G | 14 | a0001c0003 a0001c0004 a0001c0006 others(11): Show |
109 | HG00597.hp1 HG00738.hp2 HG01070.hp1 others(106): Show |
synonymous_variant | LOW | c.2142A>G | p.Val714Val | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2156/11194 | 2142/2202 | 714/733 | chr7 | 4762404 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4762567 | C | A | 1 | a0001c0002t0027 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 103 | chr7 | 4762567 | ||||||
| chr7:4762570 | C | T | 1 | a0001c0003t0099 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 106 | chr7 | 4762570 | ||||||
| chr7:4762682 | T | G | 2 | a0001c0004t0028 a0001c0004t0029 |
2 | HG00738.hp2 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*218T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 218 | chr7 | 4762682 | ||||||
| chr7:4762811 | C | T | 33 | a0001c0003t0003 a0001c0003t0008 a0001c0003t0011 others(30): Show |
58 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*347C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 347 | chr7 | 4762811 | ||||||
| chr7:4762816 | C | T | 1 | a0001c0003t0082 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 352 | chr7 | 4762816 | ||||||
| chr7:4762834 | G | A | 1 | a0001c0001t0030 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 370 | chr7 | 4762834 | ||||||
| chr7:4762843 | C | T | 1 | a0001c0003t0081 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 379 | chr7 | 4762843 | ||||||
| chr7:4762844 | G | A | 4 | a0001c0003t0012 a0001c0003t0018 a0001c0003t0031 others(1): Show |
7 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*380G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 380 | chr7 | 4762844 | ||||||
| chr7:4762888 | G | A | 3 | a0001c0001t0019 a0001c0002t0033 a0002c0012t0019 |
3 | HG01109.hp1 HG02055.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*424G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 424 | chr7 | 4762888 | ||||||
| chr7:4762965 | C | T | 1 | a0001c0003t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 501 | chr7 | 4762965 | ||||||
| chr7:4762969 | C | T | 2 | a0001c0003t0017 a0001c0003t0098 |
4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*505C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 505 | chr7 | 4762969 | ||||||
| chr7:4763292 | C | T | 1 | a0001c0003t0082 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 828 | chr7 | 4763292 | ||||||
| chr7:4763296 | C | T | 1 | a0001c0010t0079 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 832 | chr7 | 4763296 | ||||||
| chr7:4763306 | G | T | 1 | a0001c0007t0078 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*842G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 842 | chr7 | 4763306 | ||||||
| chr7:4763308 | G | T | 1 | a0001c0001t0077 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*844G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 844 | chr7 | 4763308 | ||||||
| chr7:4763363 | C | T | 2 | a0004c0016t0075 a0004c0016t0076 |
2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*899C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 899 | chr7 | 4763363 | ||||||
| chr7:4763372 | G | A | 1 | a0001c0002t0034 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*908G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 908 | chr7 | 4763372 | ||||||
| chr7:4763388 | C | T | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 924 | chr7 | 4763388 | ||||||
| chr7:4763394 | C | T | 1 | a0001c0003t0026 | 2 | NA18522.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*930C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 930 | chr7 | 4763394 | ||||||
| chr7:4763444 | C | A | 1 | a0001c0004t0035 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 980 | chr7 | 4763444 | ||||||
| chr7:4763454 | A | G | 14 | a0001c0003t0005 a0001c0003t0012 a0001c0003t0015 others(11): Show |
21 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*990A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 990 | chr7 | 4763454 | ||||||
| chr7:4763526 | C | T | 1 | a0001c0002t0069 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1062C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1062 | chr7 | 4763526 | ||||||
| chr7:4763592 | C | T | 1 | a0001c0001t0068 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1128C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1128 | chr7 | 4763592 | ||||||
| chr7:4763606 | G | A | 5 | a0001c0003t0012 a0001c0003t0018 a0001c0003t0031 others(2): Show |
8 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1142G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1142 | chr7 | 4763606 | ||||||
| chr7:4763634 | C | T | 2 | a0001c0001t0067 a0001c0002t0066 |
2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1170C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1170 | chr7 | 4763634 | ||||||
| chr7:4763644 | C | T | 2 | a0001c0006t0009 a0001c0015t0009 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1180C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1180 | chr7 | 4763644 | ||||||
| chr7:4763844 | G | A | 2 | a0001c0003t0017 a0001c0003t0098 |
4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1380G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1380 | chr7 | 4763844 | ||||||
| chr7:4763899 | G | A | 1 | a0001c0004t0035 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1435G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1435 | chr7 | 4763899 | ||||||
| chr7:4763984 | C | T | 6 | a0001c0002t0074 a0001c0003t0026 a0001c0003t0095 others(3): Show |
7 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1520C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1520 | chr7 | 4763984 | ||||||
| chr7:4763994 | C | T | 1 | a0001c0004t0029 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1530 | chr7 | 4763994 | ||||||
| chr7:4764127 | A | G | 1 | a0001c0001t0065 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1663 | chr7 | 4764127 | ||||||
| chr7:4764158 | G | C | 4 | a0001c0003t0012 a0001c0003t0018 a0001c0003t0031 others(1): Show |
7 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1694G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1694 | chr7 | 4764158 | ||||||
| chr7:4764249 | C | T | 1 | a0001c0001t0064 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1785C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1785 | chr7 | 4764249 | ||||||
| chr7:4764292 | C | T | 11 | a0001c0002t0063 a0001c0002t0074 a0001c0003t0012 others(8): Show |
15 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1828C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1828 | chr7 | 4764292 | ||||||
| chr7:4764315 | G | A | 10 | a0001c0002t0063 a0001c0003t0012 a0001c0003t0018 others(7): Show |
14 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1851G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1851 | chr7 | 4764315 | ||||||
| chr7:4764452 | G | A | 1 | a0001c0002t0036 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1988G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1988 | chr7 | 4764452 | ||||||
| chr7:4764454 | C | T | 4 | a0001c0003t0008 a0001c0003t0025 a0001c0003t0094 others(1): Show |
8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1990C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 1990 | chr7 | 4764454 | ||||||
| chr7:4764473 | G | T | 12 | a0001c0002t0074 a0001c0003t0012 a0001c0003t0018 others(9): Show |
16 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2009G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2009 | chr7 | 4764473 | ||||||
| chr7:4764498 | C | T | 12 | a0001c0002t0063 a0001c0002t0074 a0001c0003t0012 others(9): Show |
16 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2034C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2034 | chr7 | 4764498 | ||||||
| chr7:4764506 | G | A | 1 | a0001c0004t0010 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2042G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2042 | chr7 | 4764506 | ||||||
| chr7:4764572 | G | C | 5 | a0001c0003t0012 a0001c0003t0018 a0001c0003t0031 others(2): Show |
8 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2108G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2108 | chr7 | 4764572 | ||||||
| chr7:4764630 | G | A | 1 | a0006c0020t0037 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2166G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2166 | chr7 | 4764630 | ||||||
| chr7:4764639 | C | T | 3 | a0001c0003t0011 a0001c0004t0011 a0001c0004t0093 |
5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2175C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2175 | chr7 | 4764639 | ||||||
| chr7:4764697 | G | A | 5 | a0001c0003t0039 a0001c0003t0080 a0001c0003t0081 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2233G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2233 | chr7 | 4764697 | ||||||
| chr7:4764734 | C | A | 1 | a0001c0003t0026 | 2 | NA18522.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2270C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2270 | chr7 | 4764734 | ||||||
| chr7:4764752 | C | T | 2 | a0001c0003t0081 a0001c0003t0082 |
2 | HG01891.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2288C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2288 | chr7 | 4764752 | ||||||
| chr7:4764831 | C | G | 1 | a0001c0002t0069 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2367 | chr7 | 4764831 | ||||||
| chr7:4764866 | G | C | 1 | a0001c0023t0041 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2402G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2402 | chr7 | 4764866 | ||||||
| chr7:4764906 | A | G | 5 | a0001c0003t0039 a0001c0003t0062 a0001c0003t0080 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2442A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2442 | chr7 | 4764906 | ||||||
| chr7:4764920 | G | T | 6 | a0001c0002t0074 a0001c0003t0026 a0001c0003t0095 others(3): Show |
7 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2456G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2456 | chr7 | 4764920 | ||||||
| chr7:4764965 | G | A | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2501G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2501 | chr7 | 4764965 | ||||||
| chr7:4764976 | G | A | 1 | a0001c0001t0042 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2512G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2512 | chr7 | 4764976 | ||||||
| chr7:4765007 | A | G | 3 | a0001c0003t0017 a0001c0003t0092 a0001c0003t0098 |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2543 | chr7 | 4765007 | ||||||
| chr7:4765031 | G | A | 1 | a0001c0001t0043 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2567G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2567 | chr7 | 4765031 | ||||||
| chr7:4765089 | T | C | 36 | a0001c0001t0020 a0001c0001t0047 a0001c0001t0067 others(33): Show |
65 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2625T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2625 | chr7 | 4765089 | ||||||
| chr7:4765103 | G | C | 27 | a0001c0002t0063 a0001c0002t0074 a0001c0003t0005 others(24): Show |
35 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2639G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2639 | chr7 | 4765103 | ||||||
| chr7:4765113 | C | T | 2 | a0001c0001t0047 a0001c0002t0046 |
2 | HG01496.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2649C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2649 | chr7 | 4765113 | ||||||
| chr7:4765114 | G | A | 1 | a0001c0003t0070 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2650 | chr7 | 4765114 | ||||||
| chr7:4765173 | T | C | 3 | a0001c0003t0017 a0001c0003t0092 a0001c0003t0098 |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2709T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2709 | chr7 | 4765173 | ||||||
| chr7:4765261 | G | A | 12 | a0001c0001t0019 a0001c0002t0033 a0001c0003t0008 others(9): Show |
19 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2797G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2797 | chr7 | 4765261 | ||||||
| chr7:4765378 | A | G | 17 | a0001c0003t0005 a0001c0003t0012 a0001c0003t0015 others(14): Show |
26 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2914A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2914 | chr7 | 4765378 | ||||||
| chr7:4765382 | G | C | 1 | a0001c0001t0048 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2918G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2918 | chr7 | 4765382 | ||||||
| chr7:4765433 | G | A | 5 | a0001c0003t0011 a0001c0003t0024 a0001c0003t0091 others(2): Show |
8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2969G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 2969 | chr7 | 4765433 | ||||||
| chr7:4765506 | G | A | 40 | a0001c0002t0063 a0001c0002t0074 a0001c0003t0005 others(37): Show |
57 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3042 | chr7 | 4765506 | ||||||
| chr7:4765619 | G | A | 7 | a0001c0003t0039 a0001c0003t0062 a0001c0003t0080 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3155G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3155 | chr7 | 4765619 | ||||||
| chr7:4765737 | T | C | 7 | a0001c0001t0019 a0001c0002t0033 a0001c0003t0008 others(4): Show |
11 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3273T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3273 | chr7 | 4765737 | ||||||
| chr7:4765745 | C | T | 42 | a0001c0001t0019 a0001c0002t0033 a0001c0002t0063 others(39): Show |
63 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3281C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3281 | chr7 | 4765745 | ||||||
| chr7:4765850 | C | T | 7 | a0001c0003t0039 a0001c0003t0062 a0001c0003t0080 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3386C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3386 | chr7 | 4765850 | ||||||
| chr7:4766038 | C | T | 3 | a0001c0007t0004 a0001c0007t0078 a0001c0011t0004 |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3574C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3574 | chr7 | 4766038 | ||||||
| chr7:4766039 | G | A | 1 | a0001c0003t0071 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3575G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3575 | chr7 | 4766039 | ||||||
| chr7:4766055 | C | T | 7 | a0001c0002t0063 a0001c0002t0074 a0001c0003t0026 others(4): Show |
8 | HG02451.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3591C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3591 | chr7 | 4766055 | ||||||
| chr7:4766094 | G | A | 1 | a0001c0004t0038 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3630G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3630 | chr7 | 4766094 | ||||||
| chr7:4766181 | T | A | 6 | a0001c0003t0031 a0001c0006t0009 a0001c0006t0013 others(3): Show |
10 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3717T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3717 | chr7 | 4766181 | ||||||
| chr7:4766219 | CG | C | 5 | a0001c0003t0011 a0001c0003t0024 a0001c0003t0091 others(2): Show |
8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3758delG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3758 | INFO_REALIGN_3_PRIME | chr7 | 4766219 | |||||
| chr7:4766369 | G | C | 6 | a0001c0003t0005 a0001c0003t0015 a0001c0003t0072 others(3): Show |
10 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3905G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3905 | chr7 | 4766369 | ||||||
| chr7:4766401 | A | C | 15 | a0001c0003t0003 a0001c0003t0083 a0001c0003t0086 others(12): Show |
29 | HG00597.hp1 HG02698.hp2 HG03239.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3937A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 3937 | chr7 | 4766401 | ||||||
| chr7:4766567 | T | C | 9 | a0001c0003t0011 a0001c0003t0012 a0001c0003t0024 others(6): Show |
14 | HG00738.hp2 HG01978.hp1 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4103T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4103 | chr7 | 4766567 | ||||||
| chr7:4766587 | G | A | 2 | a0001c0003t0012 a0001c0003t0032 |
4 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4123G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4123 | chr7 | 4766587 | ||||||
| chr7:4766591 | C | T | 1 | a0006c0020t0037 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4127C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4127 | chr7 | 4766591 | ||||||
| chr7:4766592 | A | G | 53 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0033 others(50): Show |
79 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4128A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4128 | chr7 | 4766592 | ||||||
| chr7:4766756 | A | G | 1 | a0001c0003t0032 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4292A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4292 | chr7 | 4766756 | ||||||
| chr7:4766783 | T | C | 8 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0033 others(5): Show |
12 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4319T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4319 | chr7 | 4766783 | ||||||
| chr7:4766809 | T | A | 2 | a0001c0003t0017 a0001c0003t0098 |
4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4345T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4345 | chr7 | 4766809 | ||||||
| chr7:4766853 | G | A | 2 | a0001c0003t0012 a0001c0003t0032 |
4 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4389G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4389 | chr7 | 4766853 | ||||||
| chr7:4766870 | TGA | T | 5 | a0001c0003t0011 a0001c0003t0024 a0001c0003t0091 others(2): Show |
8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4417_*4418delGA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4417 | INFO_REALIGN_3_PRIME | chr7 | 4766870 | |||||
| chr7:4766899 | G | T | 1 | a0001c0001t0061 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4435G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4435 | chr7 | 4766899 | ||||||
| chr7:4766900 | A | G | 11 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0033 others(8): Show |
15 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4436A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4436 | chr7 | 4766900 | ||||||
| chr7:4766951 | T | C | 1 | a0001c0003t0082 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4487T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4487 | chr7 | 4766951 | ||||||
| chr7:4767044 | C | T | 1 | a0001c0002t0060 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4580C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4580 | chr7 | 4767044 | ||||||
| chr7:4767095 | A | G | 10 | a0001c0002t0074 a0001c0003t0039 a0001c0003t0062 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG01978.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4631A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4631 | chr7 | 4767095 | ||||||
| chr7:4767130 | G | A | 1 | a0001c0002t0063 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4666G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4666 | chr7 | 4767130 | ||||||
| chr7:4767211 | A | G | 8 | a0001c0003t0031 a0001c0003t0070 a0001c0003t0080 others(5): Show |
12 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4747A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4747 | chr7 | 4767211 | ||||||
| chr7:4767240 | C | T | 4 | a0001c0003t0011 a0001c0003t0024 a0001c0003t0091 others(1): Show |
7 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4776C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4776 | chr7 | 4767240 | ||||||
| chr7:4767267 | C | T | 4 | a0001c0003t0018 a0001c0003t0071 a0001c0003t0073 others(1): Show |
5 | HG02895.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4803C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4803 | chr7 | 4767267 | ||||||
| chr7:4767268 | T | C | 10 | a0001c0002t0044 a0001c0002t0074 a0001c0003t0012 others(7): Show |
13 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4804T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4804 | chr7 | 4767268 | ||||||
| chr7:4767327 | C | G | 3 | a0001c0004t0007 a0001c0004t0088 a0001c0004t0089 |
7 | NA18962.hp1 NA18995.hp2 NA19002.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4863C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4863 | chr7 | 4767327 | ||||||
| chr7:4767331 | A | C | 6 | a0001c0003t0070 a0001c0006t0009 a0001c0006t0013 others(3): Show |
10 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4867A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4867 | chr7 | 4767331 | ||||||
| chr7:4767334 | G | A | 1 | a0001c0001t0049 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4870G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 4870 | chr7 | 4767334 | ||||||
| chr7:4767544 | T | C | 1 | a0001c0002t0050 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5080T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5080 | chr7 | 4767544 | ||||||
| chr7:4767578 | C | T | 1 | a0001c0001t0059 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5114C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5114 | chr7 | 4767578 | ||||||
| chr7:4767592 | G | T | 10 | a0001c0002t0074 a0001c0003t0012 a0001c0003t0032 others(7): Show |
12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5128G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5128 | chr7 | 4767592 | ||||||
| chr7:4767620 | G | A | 14 | a0001c0001t0019 a0001c0002t0033 a0001c0003t0008 others(11): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5156G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5156 | chr7 | 4767620 | ||||||
| chr7:4767692 | CCTTTT | C | 3 | a0001c0003t0095 a0001c0003t0096 a0001c0004t0097 |
3 | HG02451.hp1 HG02965.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5235_*5239delTTTT others(1): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5235 | INFO_REALIGN_3_PRIME | chr7 | 4767692 | |||||
| chr7:4767790 | C | T | 1 | a0001c0004t0045 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5326C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5326 | chr7 | 4767790 | ||||||
| chr7:4767814 | C | G | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5350C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5350 | chr7 | 4767814 | ||||||
| chr7:4767865 | C | T | 7 | a0001c0001t0019 a0001c0002t0033 a0001c0003t0008 others(4): Show |
11 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5401C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5401 | chr7 | 4767865 | ||||||
| chr7:4768111 | TCACTGAC others(313): Show |
T | 11 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0033 others(8): Show |
20 | HG01081.hp2 HG01109.hp1 HG01496.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5661_*5980del | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5661 | INFO_REALIGN_3_PRIME | chr7 | 4768111 | |||||
| chr7:4768121 | C | CT | 26 | a0001c0001t0001 a0001c0001t0021 a0001c0001t0042 others(23): Show |
49 | HG00597.hp2 HG00735.hp2 HG01099.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*5686dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768121 | C | CTT | 6 | a0001c0002t0002 a0001c0002t0069 a0001c0003t0002 others(3): Show |
6 | HG01123.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5685_*5686dupTT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768121 | C | CTTTTTT | 7 | a0001c0004t0003 a0001c0004t0007 a0001c0004t0088 others(4): Show |
11 | HG00597.hp1 HG03654.hp1 HG04184.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5681_*5686dupTTTT others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768121 | C | CTTTTTTT | 5 | a0001c0003t0003 a0001c0003t0083 a0001c0004t0003 others(2): Show |
7 | HG03688.hp2 NA18747.hp2 NA18940.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5680_*5686dupTTTT others(3): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768121 | C | CTTTTTTT others(4): Show |
1 | a0001c0003t0026 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5676_*5686dupTTTT others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768121 | C | CTTTTTTT others(5): Show |
1 | a0001c0003t0026 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5675_*5686dupTTTT others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5687 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768121 | CT | C | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0003t0005 others(10): Show |
15 | HG00323.hp2 HG01070.hp2 HG01256.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5686delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5686 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768121 | CTT | C | 5 | a0001c0003t0012 a0001c0003t0032 a0001c0003t0039 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5685_*5686delTT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5685 | INFO_REALIGN_3_PRIME | chr7 | 4768121 | |||||
| chr7:4768155 | C | T | 8 | a0001c0002t0074 a0001c0003t0012 a0001c0003t0032 others(5): Show |
10 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5691C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5691 | chr7 | 4768155 | ||||||
| chr7:4768172 | G | A | 5 | a0001c0003t0011 a0001c0003t0024 a0001c0003t0091 others(2): Show |
8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5708G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5708 | chr7 | 4768172 | ||||||
| chr7:4768195 | T | C | 7 | a0001c0002t0074 a0001c0003t0011 a0001c0003t0024 others(4): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5731T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5731 | chr7 | 4768195 | ||||||
| chr7:4768199 | C | T | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5735C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5735 | chr7 | 4768199 | ||||||
| chr7:4768201 | C | T | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5737C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5737 | chr7 | 4768201 | ||||||
| chr7:4768202 | G | A | 5 | a0001c0003t0011 a0001c0003t0024 a0001c0003t0091 others(2): Show |
8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5738G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5738 | chr7 | 4768202 | ||||||
| chr7:4768210 | G | T | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5746G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5746 | chr7 | 4768210 | ||||||
| chr7:4768220 | C | T | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5756C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5756 | chr7 | 4768220 | ||||||
| chr7:4768222 | T | C | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5758T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5758 | chr7 | 4768222 | ||||||
| chr7:4768233 | C | T | 1 | a0001c0019t0090 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5769C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5769 | chr7 | 4768233 | ||||||
| chr7:4768277 | C | T | 3 | a0001c0003t0083 a0001c0003t0086 a0001c0009t0003 |
5 | NA18747.hp2 NA18969.hp2 NA19060.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5813C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5813 | chr7 | 4768277 | ||||||
| chr7:4768282 | G | A | 1 | a0001c0001t0001 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5818G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5818 | chr7 | 4768282 | ||||||
| chr7:4768284 | T | C | 1 | a0001c0001t0001 | 4 | NA18944.hp1 NA18954.hp1 NA18985.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5820T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5820 | chr7 | 4768284 | ||||||
| chr7:4768293 | C | A | 1 | a0001c0002t0001 | 2 | HG00735.hp2 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5829C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5829 | chr7 | 4768293 | ||||||
| chr7:4768322 | C | T | 1 | a0001c0001t0001 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5858C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5858 | chr7 | 4768322 | ||||||
| chr7:4768356 | T | C | 1 | a0001c0003t0017 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5892T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5892 | chr7 | 4768356 | ||||||
| chr7:4768368 | G | A | 1 | a0001c0019t0090 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5904G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5904 | chr7 | 4768368 | ||||||
| chr7:4768379 | G | A | 5 | a0001c0003t0039 a0001c0003t0062 a0001c0003t0080 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5915G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5915 | chr7 | 4768379 | ||||||
| chr7:4768423 | C | T | 2 | a0001c0001t0001 a0001c0002t0001 |
4 | HG00323.hp1 HG01515.hp1 HG02602.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5959C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5959 | chr7 | 4768423 | ||||||
| chr7:4768427 | C | T | 2 | a0001c0001t0001 a0001c0002t0001 |
4 | HG00323.hp1 HG01515.hp1 HG02602.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5963C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5963 | chr7 | 4768427 | ||||||
| chr7:4768428 | G | A | 4 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0036 others(1): Show |
6 | HG02074.hp2 HG02132.hp2 HG02523.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5964G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 5964 | chr7 | 4768428 | ||||||
| chr7:4768467 | G | A | 1 | a0001c0003t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6003G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6003 | chr7 | 4768467 | ||||||
| chr7:4768538 | C | T | 4 | a0001c0004t0045 a0001c0007t0004 a0001c0007t0078 others(1): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6074C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6074 | chr7 | 4768538 | ||||||
| chr7:4768563 | C | T | 8 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0033 others(5): Show |
12 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6099C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6099 | chr7 | 4768563 | ||||||
| chr7:4768715 | C | T | 1 | a0001c0001t0058 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6251C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6251 | chr7 | 4768715 | ||||||
| chr7:4768738 | A | G | 3 | a0001c0003t0017 a0001c0003t0092 a0001c0003t0098 |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6274A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6274 | chr7 | 4768738 | ||||||
| chr7:4768772 | C | T | 1 | a0001c0003t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6308C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6308 | chr7 | 4768772 | ||||||
| chr7:4768773 | G | A | 9 | a0001c0001t0019 a0001c0003t0008 a0001c0003t0025 others(6): Show |
18 | HG01081.hp2 HG01109.hp1 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*6309G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6309 | chr7 | 4768773 | ||||||
| chr7:4768936 | G | T | 5 | a0001c0001t0020 a0001c0001t0067 a0001c0002t0020 others(2): Show |
5 | HG01891.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6472G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6472 | chr7 | 4768936 | ||||||
| chr7:4769047 | A | T | 47 | a0001c0001t0019 a0001c0001t0047 a0001c0001t0057 others(44): Show |
72 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*6583A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6583 | chr7 | 4769047 | ||||||
| chr7:4769054 | G | A | 1 | a0001c0002t0074 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6590G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6590 | chr7 | 4769054 | ||||||
| chr7:4769061 | C | T | 45 | a0001c0001t0019 a0001c0001t0047 a0001c0001t0057 others(42): Show |
70 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*6597C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6597 | chr7 | 4769061 | ||||||
| chr7:4769317 | C | G | 6 | a0001c0003t0005 a0001c0003t0015 a0001c0003t0072 others(3): Show |
10 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6853C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6853 | chr7 | 4769317 | ||||||
| chr7:4769318 | C | T | 4 | a0001c0002t0063 a0001c0007t0004 a0001c0007t0078 others(1): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6854C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6854 | chr7 | 4769318 | ||||||
| chr7:4769322 | C | G | 27 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0002 others(24): Show |
47 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*6858C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6858 | chr7 | 4769322 | ||||||
| chr7:4769355 | G | C | 3 | a0001c0007t0004 a0001c0007t0078 a0001c0011t0004 |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6891G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6891 | chr7 | 4769355 | ||||||
| chr7:4769372 | A | G | 54 | a0001c0001t0019 a0001c0001t0023 a0001c0001t0047 others(51): Show |
95 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*6908A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6908 | chr7 | 4769372 | ||||||
| chr7:4769401 | G | A | 2 | a0001c0001t0047 a0001c0002t0033 |
2 | HG02055.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6937G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6937 | chr7 | 4769401 | ||||||
| chr7:4769419 | G | A | 8 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0033 others(5): Show |
12 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6955G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6955 | chr7 | 4769419 | ||||||
| chr7:4769443 | CT | C | 6 | a0001c0001t0006 a0001c0001t0042 a0001c0002t0006 others(3): Show |
8 | HG01175.hp1 HG02074.hp2 HG02132.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6992delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 6992 | INFO_REALIGN_3_PRIME | chr7 | 4769443 | |||||
| chr7:4769465 | G | A | 2 | a0001c0003t0082 a0001c0003t0099 |
2 | HG02922.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7001G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7001 | chr7 | 4769465 | ||||||
| chr7:4769592 | A | C | 26 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0002 others(23): Show |
47 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*7128A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7128 | chr7 | 4769592 | ||||||
| chr7:4769686 | C | T | 1 | a0001c0008t0087 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7222C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7222 | chr7 | 4769686 | ||||||
| chr7:4769705 | T | C | 23 | a0001c0001t0021 a0001c0002t0063 a0001c0002t0066 others(20): Show |
40 | HG00597.hp1 HG01081.hp2 HG01175.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*7241T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7241 | chr7 | 4769705 | ||||||
| chr7:4769732 | C | T | 1 | a0001c0001t0055 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7268C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7268 | chr7 | 4769732 | ||||||
| chr7:4769806 | T | G | 62 | a0001c0001t0019 a0001c0001t0021 a0001c0001t0047 others(59): Show |
109 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*7342T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7342 | chr7 | 4769806 | ||||||
| chr7:4769876 | T | G | 2 | a0001c0006t0009 a0001c0015t0009 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7412T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7412 | chr7 | 4769876 | ||||||
| chr7:4769911 | G | A | 1 | a0001c0001t0055 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7447G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7447 | chr7 | 4769911 | ||||||
| chr7:4769918 | A | AGAGTGCA others(16): Show |
1 | a0004c0016t0075 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7456_*7478dupAGTG others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7479 | INFO_REALIGN_3_PRIME | chr7 | 4769918 | |||||
| chr7:4770029 | G | T | 58 | a0001c0001t0019 a0001c0001t0021 a0001c0001t0047 others(55): Show |
103 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*7565G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7565 | chr7 | 4770029 | ||||||
| chr7:4770066 | A | G | 3 | a0001c0007t0004 a0001c0007t0078 a0001c0011t0004 |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7602A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7602 | chr7 | 4770066 | ||||||
| chr7:4770222 | A | C | 1 | a0001c0001t0054 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7758A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7758 | chr7 | 4770222 | ||||||
| chr7:4770301 | G | A | 5 | a0001c0003t0011 a0001c0003t0024 a0001c0003t0091 others(2): Show |
8 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7837G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7837 | chr7 | 4770301 | ||||||
| chr7:4770316 | C | T | 5 | a0001c0002t0044 a0001c0003t0080 a0001c0003t0081 others(2): Show |
5 | HG01891.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7852C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7852 | chr7 | 4770316 | ||||||
| chr7:4770319 | G | C | 5 | a0001c0002t0044 a0001c0003t0080 a0001c0003t0081 others(2): Show |
5 | HG01891.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7855G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7855 | chr7 | 4770319 | ||||||
| chr7:4770389 | G | C | 2 | a0001c0003t0025 a0001c0003t0094 |
3 | HG03098.hp1 HG03579.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7925G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7925 | chr7 | 4770389 | ||||||
| chr7:4770391 | C | G | 1 | a0001c0001t0056 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7927C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7927 | chr7 | 4770391 | ||||||
| chr7:4770392 | G | A | 1 | a0001c0003t0082 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7928G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 7928 | chr7 | 4770392 | ||||||
| chr7:4770479 | C | T | 1 | a0001c0001t0021 | 2 | HG01175.hp2 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8015C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8015 | chr7 | 4770479 | ||||||
| chr7:4770566 | CTCT | C | 12 | a0001c0001t0021 a0001c0003t0005 a0001c0003t0015 others(9): Show |
18 | HG01175.hp2 HG01515.hp2 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8107_*8109delCTT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8107 | INFO_REALIGN_3_PRIME | chr7 | 4770566 | |||||
| chr7:4770569 | T | C | 3 | a0001c0002t0002 a0001c0003t0002 a0002c0012t0002 |
13 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8105T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8105 | chr7 | 4770569 | ||||||
| chr7:4770593 | T | C | 21 | a0001c0001t0019 a0001c0001t0021 a0001c0001t0047 others(18): Show |
32 | HG01109.hp1 HG01175.hp2 HG01515.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*8129T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8129 | chr7 | 4770593 | ||||||
| chr7:4770652 | G | A | 1 | a0001c0001t0022 | 2 | NA18980.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8188G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8188 | chr7 | 4770652 | ||||||
| chr7:4770685 | G | A | 1 | a0001c0001t0056 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8221G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8221 | chr7 | 4770685 | ||||||
| chr7:4770795 | T | C | 2 | a0001c0005t0014 a0005c0025t0014 |
3 | HG00621.hp2 HG01981.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8331T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8331 | chr7 | 4770795 | ||||||
| chr7:4770831 | G | A | 1 | a0001c0003t0098 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8367G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8367 | chr7 | 4770831 | ||||||
| chr7:4770864 | G | GGT | 6 | a0001c0001t0001 a0001c0003t0017 a0001c0003t0032 others(3): Show |
9 | HG00597.hp1 HG02109.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8437_*8438dupGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770864 | G | GGTGT | 10 | a0001c0002t0002 a0001c0003t0002 a0001c0003t0017 others(7): Show |
20 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8435_*8438dupGTGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770864 | G | GGTGTGT | 7 | a0001c0002t0002 a0001c0003t0025 a0001c0003t0070 others(4): Show |
9 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8433_*8438dupGTGT others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770864 | GGT | G | 15 | a0001c0001t0001 a0001c0001t0048 a0001c0002t0001 others(12): Show |
22 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*8437_*8438delGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8437 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770864 | GGTGT | G | 50 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0020 others(47): Show |
133 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*8435_*8438delGTGT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8435 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770864 | GGTGTGTG others(1): Show |
G | 5 | a0001c0003t0026 a0001c0003t0073 a0001c0004t0035 others(2): Show |
6 | HG00323.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8431_*8438delGTGT others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8431 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770864 | GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0001 a0001c0001t0077 a0001c0002t0001 |
4 | HG02056.hp2 HG02080.hp1 HG02135.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8429_*8438delGTGT others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8429 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770864 | GGTGTGTG others(11): Show |
G | 2 | a0004c0016t0075 a0004c0016t0076 |
2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8421_*8438delGTGT others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8421 | INFO_REALIGN_3_PRIME | chr7 | 4770864 | |||||
| chr7:4770884 | T | G | 2 | a0004c0016t0075 a0004c0016t0076 |
2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8420T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8420 | chr7 | 4770884 | ||||||
| chr7:4770895 | G | A | 1 | a0001c0003t0091 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8431G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8431 | chr7 | 4770895 | ||||||
| chr7:4770899 | G | A | 1 | a0001c0001t0001 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8435G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8435 | chr7 | 4770899 | ||||||
| chr7:4770903 | A | G | 2 | a0001c0003t0017 a0001c0003t0098 |
4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8439A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | chr7 | 4770903 | ||||||
| chr7:4770903 | A | T | 2 | a0001c0003t0024 a0001c0019t0090 |
2 | HG03453.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8439A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8439 | chr7 | 4770903 | ||||||
| chr7:4770905 | T | A | 2 | a0001c0003t0017 a0001c0003t0098 |
4 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8441T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8441 | chr7 | 4770905 | ||||||
| chr7:4770923 | G | A | 1 | a0001c0001t0051 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8459G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8459 | chr7 | 4770923 | ||||||
| chr7:4770927 | G | A | 1 | a0001c0003t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8463G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8463 | chr7 | 4770927 | ||||||
| chr7:4770936 | AT | A | 26 | a0001c0002t0002 a0001c0002t0063 a0001c0003t0002 others(23): Show |
52 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*8477delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8477 | INFO_REALIGN_3_PRIME | chr7 | 4770936 | |||||
| chr7:4770978 | C | T | 1 | a0001c0001t0052 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8514C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8514 | chr7 | 4770978 | ||||||
| chr7:4771081 | G | A | 2 | a0001c0003t0012 a0001c0003t0032 |
4 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8617G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8617 | chr7 | 4771081 | ||||||
| chr7:4771103 | C | G | 1 | a0001c0023t0041 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8639C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8639 | chr7 | 4771103 | ||||||
| chr7:4771170 | A | G | 62 | a0001c0001t0019 a0001c0001t0021 a0001c0001t0047 others(59): Show |
109 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*8706A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8706 | chr7 | 4771170 | ||||||
| chr7:4771208 | TTAA | T | 7 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0033 others(4): Show |
11 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8748_*8750delTAA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 9/9 | 8748 | INFO_REALIGN_3_PRIME | chr7 | 4771208 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4682884 | A | AC | 5 | a0001c0001t0001g0006 a0001c0002t0001g0009 a0001c0003t0081g0007 others(2): Show |
5 | HG01891.hp2 HG02080.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+21dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4682884 | ||||||
| chr7:4682885 | C | A | 2 | a0001c0003t0031g0005 a0001c0003t0096g0004 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.560+17C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4682885 | |||||||
| chr7:4682979 | C | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(53): Show |
57 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.560+111C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4682979 | |||||||
| chr7:4682991 | C | T | 5 | a0002c0012t0002g0291 a0002c0012t0019g0290 a0002c0013t0008g0288 others(2): Show |
5 | HG01109.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+123C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4682991 | |||||||
| chr7:4683059 | A | G | 3 | a0001c0002t0020g0285 a0001c0003t0011g0284 a0001c0003t0094g0286 |
3 | HG02055.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+191A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683059 | |||||||
| chr7:4683076 | C | T | 8 | a0001c0002t0020g0285 a0001c0003t0011g0284 a0001c0003t0094g0286 others(5): Show |
8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+208C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683076 | |||||||
| chr7:4683098 | T | A | 1 | a0001c0002t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+230T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683098 | |||||||
| chr7:4683142 | C | G | 3 | a0001c0002t0020g0285 a0001c0003t0011g0284 a0001c0003t0094g0286 |
3 | HG02055.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+274C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683142 | |||||||
| chr7:4683181 | C | T | 1 | a0001c0003t0018g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+313C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683181 | |||||||
| chr7:4683198 | C | T | 4 | a0001c0002t0002g0282 a0001c0003t0070g0281 a0001c0004t0038g0010 others(1): Show |
4 | HG01496.hp2 HG02970.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+330C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683198 | |||||||
| chr7:4683259 | C | T | 1 | a0002c0012t0002g0291 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.560+391C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683259 | |||||||
| chr7:4683291 | C | G | 1 | a0001c0015t0009g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.560+423C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683291 | |||||||
| chr7:4683293 | C | T | 2 | a0001c0003t0031g0005 a0001c0003t0096g0004 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.560+425C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683293 | |||||||
| chr7:4683300 | T | C | 8 | a0001c0002t0020g0285 a0001c0003t0011g0284 a0001c0003t0094g0286 others(5): Show |
8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+432T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683300 | |||||||
| chr7:4683311 | C | T | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.560+443C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683311 | |||||||
| chr7:4683410 | A | AC | 12 | a0001c0001t0001g0006 a0001c0001t0001g0269 a0001c0002t0001g0276 others(9): Show |
12 | HG00735.hp2 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.560+547dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4683410 | ||||||
| chr7:4683449 | G | A | 48 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(45): Show |
49 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.560+581G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683449 | |||||||
| chr7:4683522 | T | C | 53 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(50): Show |
54 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.560+654T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683522 | |||||||
| chr7:4683710 | G | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(44): Show |
48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.560+842G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683710 | |||||||
| chr7:4683712 | T | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(44): Show |
48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.560+844T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683712 | |||||||
| chr7:4683903 | G | A | 16 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0055 others(13): Show |
16 | HG00140.hp2 HG01074.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.560+1035G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683903 | |||||||
| chr7:4683976 | G | A | 2 | a0001c0003t0001g0113 a0001c0004t0001g0114 |
2 | HG01070.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.560+1108G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4683976 | |||||||
| chr7:4684056 | C | T | 2 | a0001c0003t0018g0283 a0001c0006t0009g0002 |
3 | HG01070.hp2 HG01071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.560+1188C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684056 | |||||||
| chr7:4684410 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.560+1542T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684410 | |||||||
| chr7:4684578 | A | C | 2 | a0001c0002t0020g0285 a0001c0003t0094g0286 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+1710A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684578 | |||||||
| chr7:4684623 | G | C | 3 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0003t0012g0067 |
3 | HG02572.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.560+1755G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684623 | |||||||
| chr7:4684670 | C | T | 1 | a0001c0002t0069g0268 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.560+1802C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684670 | |||||||
| chr7:4684726 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.560+1858C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684726 | |||||||
| chr7:4684742 | G | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG00735.hp1 HG01261.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+1874G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684742 | |||||||
| chr7:4684766 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.560+1898G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684766 | |||||||
| chr7:4684876 | G | T | 1 | a0001c0004t0085g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.560+2008G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684876 | |||||||
| chr7:4684962 | C | T | 1 | a0001c0001t0058g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.560+2094C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684962 | |||||||
| chr7:4684976 | G | T | 1 | a0001c0002t0033g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+2108G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4684976 | |||||||
| chr7:4685107 | G | T | 9 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | HG01192.hp1 HG01928.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+2239G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685107 | |||||||
| chr7:4685133 | T | G | 4 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0003t0011g0284 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+2265T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685133 | |||||||
| chr7:4685171 | A | G | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0002t0001g0277 |
3 | HG02145.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.560+2303A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685171 | |||||||
| chr7:4685208 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.560+2340A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685208 | |||||||
| chr7:4685221 | C | CT | 15 | a0001c0001t0001g0046 a0001c0001t0001g0063 a0001c0001t0001g0102 others(12): Show |
15 | HG00597.hp1 HG00673.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.560+2373dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685221 | ||||||
| chr7:4685221 | CT | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0108 others(144): Show |
147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.560+2373delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685221 | ||||||
| chr7:4685301 | A | G | 1 | a0001c0003t0011g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+2433A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685301 | |||||||
| chr7:4685349 | G | A | 1 | a0001c0002t0033g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+2481G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685349 | |||||||
| chr7:4685399 | A | G | 3 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0003t0012g0067 |
3 | HG02572.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.560+2531A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685399 | |||||||
| chr7:4685517 | C | T | 1 | a0001c0002t0033g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+2649C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685517 | |||||||
| chr7:4685525 | CT | C | 26 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0055 others(23): Show |
26 | HG00140.hp2 HG01070.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.560+2676delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685525 | ||||||
| chr7:4685600 | C | CTTTTTTG others(10): Show |
1 | a0001c0004t0007g0008 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.560+2733_560+2749d others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685600 | ||||||
| chr7:4685675 | CCTCACGC others(14): Show |
C | 1 | a0001c0004t0005g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.560+2810_560+2830d others(23): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685675 | ||||||
| chr7:4685680 | C | A | 33 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(30): Show |
33 | HG01192.hp1 HG01496.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.560+2812C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685680 | |||||||
| chr7:4685681 | G | A | 1 | a0001c0001t0048g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+2813G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685681 | |||||||
| chr7:4685867 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.560+2999C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685867 | |||||||
| chr7:4685958 | G | GA | 9 | a0001c0001t0001g0014 a0001c0001t0001g0235 a0001c0001t0023g0015 others(6): Show |
9 | HG00597.hp2 HG02135.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+3102dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685958 | ||||||
| chr7:4685972 | C | CA | 3 | a0001c0001t0001g0124 a0001c0003t0011g0236 a0001c0008t0087g0271 |
3 | HG02572.hp1 NA18985.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.560+3110dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4685972 | ||||||
| chr7:4685979 | C | T | 4 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0003t0011g0284 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+3111C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4685979 | |||||||
| chr7:4686071 | T | A | 36 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(33): Show |
36 | HG01192.hp1 HG01496.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.560+3203T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686071 | |||||||
| chr7:4686289 | G | A | 23 | a0001c0001t0001g0269 a0001c0002t0044g0087 a0001c0002t0063g0253 others(20): Show |
24 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.560+3421G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686289 | |||||||
| chr7:4686393 | G | A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(35): Show |
39 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.560+3525G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686393 | |||||||
| chr7:4686418 | T | G | 1 | a0001c0004t0007g0008 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.560+3550T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686418 | |||||||
| chr7:4686492 | A | G | 1 | a0001c0001t0059g0231 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.560+3624A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686492 | |||||||
| chr7:4686593 | G | A | 1 | a0001c0002t0002g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.560+3725G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686593 | |||||||
| chr7:4686601 | G | A | 21 | a0001c0001t0001g0110 a0001c0001t0019g0241 a0001c0001t0047g0249 others(18): Show |
21 | HG01496.hp1 HG01884.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+3733G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686601 | |||||||
| chr7:4686767 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.560+3899A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686767 | |||||||
| chr7:4686778 | G | A | 2 | a0001c0003t0018g0283 a0001c0006t0009g0002 |
3 | HG01070.hp2 HG01071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.560+3910G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686778 | |||||||
| chr7:4686936 | TC | T | 42 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(39): Show |
42 | HG01192.hp1 HG01496.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+4069delC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686936 | |||||||
| chr7:4686937 | C | T | 20 | a0001c0001t0001g0269 a0001c0001t0047g0249 a0001c0002t0002g0068 others(17): Show |
21 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+4069C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686937 | |||||||
| chr7:4686975 | G | C | 61 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(58): Show |
62 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.560+4107G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686975 | |||||||
| chr7:4686996 | G | A | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+4128G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4686996 | |||||||
| chr7:4687026 | G | A | 1 | a0001c0001t0058g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.560+4158G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687026 | |||||||
| chr7:4687135 | T | C | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.560+4267T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687135 | |||||||
| chr7:4687183 | C | T | 1 | a0001c0002t0033g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+4315C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687183 | |||||||
| chr7:4687194 | A | G | 7 | a0001c0002t0033g0103 a0001c0011t0004g0251 a0002c0012t0002g0291 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+4326A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687194 | |||||||
| chr7:4687222 | A | G | 1 | a0001c0026t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.560+4354A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687222 | |||||||
| chr7:4687224 | G | A | 1 | a0001c0026t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.560+4356G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687224 | |||||||
| chr7:4687337 | G | T | 1 | a0001c0008t0087g0271 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.560+4469G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687337 | |||||||
| chr7:4687438 | G | A | 3 | a0002c0012t0019g0290 a0002c0013t0008g0288 a0002c0013t0015g0287 |
3 | HG01109.hp1 HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.560+4570G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687438 | |||||||
| chr7:4687440 | A | C | 3 | a0002c0012t0019g0290 a0002c0013t0008g0288 a0002c0013t0015g0287 |
3 | HG01109.hp1 HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.560+4572A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687440 | |||||||
| chr7:4687443 | T | C | 3 | a0002c0012t0019g0290 a0002c0013t0008g0288 a0002c0013t0015g0287 |
3 | HG01109.hp1 HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.560+4575T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687443 | |||||||
| chr7:4687500 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.560+4632C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687500 | |||||||
| chr7:4687638 | C | T | 12 | a0001c0001t0001g0269 a0001c0002t0044g0087 a0001c0003t0015g0086 others(9): Show |
13 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.560+4770C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687638 | |||||||
| chr7:4687718 | C | G | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+4850C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687718 | |||||||
| chr7:4687750 | A | C | 9 | a0001c0002t0044g0087 a0001c0003t0012g0229 a0001c0003t0015g0086 others(6): Show |
9 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+4882A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687750 | |||||||
| chr7:4687923 | G | T | 1 | a0001c0004t0035g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+5055G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687923 | |||||||
| chr7:4687974 | C | T | 1 | a0001c0004t0003g0228 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.560+5106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4687974 | |||||||
| chr7:4688159 | C | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0004t0010g0001 others(1): Show |
5 | HG02602.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+5291C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688159 | |||||||
| chr7:4688237 | A | C | 2 | a0001c0003t0011g0081 a0001c0003t0011g0284 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.560+5369A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688237 | |||||||
| chr7:4688266 | T | TA | 7 | a0001c0001t0001g0016 a0001c0002t0001g0107 a0001c0003t0081g0007 others(4): Show |
7 | HG01261.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+5414dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688266 | ||||||
| chr7:4688266 | TA | T | 86 | a0001c0001t0001g0040 a0001c0001t0001g0054 a0001c0001t0001g0055 others(83): Show |
88 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.560+5414delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688266 | ||||||
| chr7:4688310 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.560+5442A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688310 | |||||||
| chr7:4688311 | T | C | 15 | a0001c0002t0002g0125 a0001c0002t0002g0126 a0001c0002t0002g0245 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.560+5443T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688311 | |||||||
| chr7:4688349 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0055 others(139): Show |
143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.560+5481A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688349 | |||||||
| chr7:4688409 | A | AT | 13 | a0001c0001t0047g0249 a0001c0002t0002g0068 a0001c0002t0002g0227 others(10): Show |
13 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.560+5550dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688409 | ||||||
| chr7:4688465 | A | G | 59 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 others(56): Show |
60 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.560+5597A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688465 | |||||||
| chr7:4688550 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.560+5682G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688550 | |||||||
| chr7:4688633 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.560+5765C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688633 | |||||||
| chr7:4688672 | G | A | 5 | a0001c0001t0006g0041 a0001c0002t0002g0243 a0001c0002t0020g0285 others(2): Show |
5 | HG01081.hp2 HG02451.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+5804G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688672 | |||||||
| chr7:4688693 | T | C | 1 | a0001c0003t0012g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+5825T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688693 | |||||||
| chr7:4688713 | T | A | 1 | a0001c0003t0012g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+5845T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688713 | |||||||
| chr7:4688714 | G | A | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+5846G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688714 | |||||||
| chr7:4688812 | C | T | 1 | a0001c0007t0004g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.560+5944C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688812 | |||||||
| chr7:4688835 | GT | G | 4 | a0001c0002t0002g0069 a0001c0004t0038g0010 a0001c0007t0004g0234 others(1): Show |
4 | HG01496.hp2 HG02630.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+5971delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688835 | ||||||
| chr7:4688944 | A | G | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.560+6076A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688944 | |||||||
| chr7:4688978 | A | C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0046 others(25): Show |
28 | HG00140.hp2 HG00558.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.560+6110A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688978 | |||||||
| chr7:4688979 | C | CT | 7 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0049g0039 others(4): Show |
7 | HG01258.hp2 HG02056.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+6125dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4688979 | ||||||
| chr7:4688980 | T | C | 1 | a0001c0002t0001g0051 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.560+6112T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4688980 | |||||||
| chr7:4689137 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+6269C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689137 | |||||||
| chr7:4689186 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.560+6318C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689186 | |||||||
| chr7:4689317 | G | C | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+6449G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689317 | |||||||
| chr7:4689640 | A | G | 2 | a0001c0002t0001g0222 a0001c0002t0001g0276 |
2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.560+6772A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689640 | |||||||
| chr7:4689772 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.560+6904C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689772 | |||||||
| chr7:4689821 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.560+6953C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689821 | |||||||
| chr7:4689892 | C | T | 2 | a0001c0003t0071g0250 a0001c0003t0094g0286 |
2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.560+7024C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4689892 | |||||||
| chr7:4690002 | G | T | 1 | a0001c0002t0001g0191 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.560+7134G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690002 | |||||||
| chr7:4690052 | G | A | 1 | a0001c0002t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+7184G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690052 | |||||||
| chr7:4690121 | G | C | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0002t0001g0277 |
3 | HG02145.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.560+7253G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690121 | |||||||
| chr7:4690232 | G | C | 1 | a0001c0001t0048g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+7364G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690232 | |||||||
| chr7:4690314 | G | A | 2 | a0001c0002t0001g0127 a0001c0002t0001g0191 |
2 | HG02056.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.560+7446G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690314 | |||||||
| chr7:4690570 | A | G | 4 | a0001c0003t0024g0071 a0001c0003t0024g0088 a0001c0004t0011g0255 others(1): Show |
4 | HG02615.hp2 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+7702A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690570 | |||||||
| chr7:4690620 | T | C | 1 | a0001c0001t0068g0052 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.560+7752T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690620 | |||||||
| chr7:4690646 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.560+7778G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690646 | |||||||
| chr7:4690713 | T | TA | 13 | a0001c0002t0002g0069 a0001c0002t0020g0285 a0001c0002t0033g0103 others(10): Show |
13 | HG01081.hp2 HG01109.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.560+7845_560+7846i others(3): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690713 | |||||||
| chr7:4690904 | T | G | 11 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0054g0129 others(8): Show |
11 | HG00140.hp1 HG01070.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.560+8036T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4690904 | |||||||
| chr7:4691077 | T | C | 1 | a0001c0004t0097g0248 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+8209T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691077 | |||||||
| chr7:4691164 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.560+8296G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691164 | |||||||
| chr7:4691239 | TTTTGCTT others(6): Show |
T | 1 | a0001c0001t0030g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.560+8372_560+8384d others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691239 | |||||||
| chr7:4691351 | C | T | 10 | a0001c0001t0019g0241 a0001c0002t0002g0227 a0001c0002t0002g0239 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+8483C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691351 | |||||||
| chr7:4691352 | A | G | 40 | a0001c0001t0001g0013 a0001c0001t0019g0241 a0001c0001t0067g0094 others(37): Show |
40 | HG01081.hp2 HG01109.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.560+8484A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691352 | |||||||
| chr7:4691446 | T | A | 1 | a0001c0003t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+8578T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691446 | |||||||
| chr7:4691482 | CTGCCACC others(1055): Show |
C | 1 | a0001c0004t0010g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560+8638_560+9699d others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4691482 | ||||||
| chr7:4691483 | T | C | 49 | a0001c0001t0001g0013 a0001c0001t0019g0241 a0001c0001t0067g0094 others(46): Show |
50 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.560+8615T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691483 | |||||||
| chr7:4691523 | C | T | 4 | a0001c0002t0020g0285 a0001c0003t0062g0072 a0001c0003t0091g0278 others(1): Show |
4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+8655C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691523 | |||||||
| chr7:4691540 | C | T | 1 | a0001c0002t0023g0048 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.560+8672C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691540 | |||||||
| chr7:4691745 | G | A | 1 | a0001c0001t0059g0231 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.560+8877G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691745 | |||||||
| chr7:4691763 | T | C | 16 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0069g0268 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+8895T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691763 | |||||||
| chr7:4691818 | G | A | 3 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0004t0005g0263 |
3 | HG02257.hp1 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.560+8950G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4691818 | |||||||
| chr7:4692049 | G | A | 2 | a0001c0001t0051g0025 a0001c0002t0001g0257 |
2 | HG01433.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.560+9181G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692049 | |||||||
| chr7:4692068 | G | A | 63 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(60): Show |
64 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.560+9200G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692068 | |||||||
| chr7:4692080 | A | G | 10 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0001c0003t0071g0250 others(7): Show |
10 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+9212A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692080 | |||||||
| chr7:4692115 | A | C | 11 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0069g0268 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+9247A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692115 | |||||||
| chr7:4692275 | A | G | 1 | a0001c0003t0018g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+9407A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692275 | |||||||
| chr7:4692346 | G | A | 7 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0001c0006t0013g0075 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+9478G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692346 | |||||||
| chr7:4692364 | C | T | 2 | a0001c0003t0012g0229 a0001c0003t0095g0073 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+9496C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692364 | |||||||
| chr7:4692623 | A | G | 21 | a0001c0002t0002g0282 a0001c0002t0020g0285 a0001c0002t0033g0103 others(18): Show |
21 | HG01081.hp2 HG01109.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+9755A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692623 | |||||||
| chr7:4692704 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0042g0139 |
2 | HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.560+9836G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692704 | |||||||
| chr7:4692752 | T | C | 66 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(63): Show |
67 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.560+9884T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692752 | |||||||
| chr7:4692766 | A | T | 1 | a0001c0004t0007g0233 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.560+9898A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692766 | |||||||
| chr7:4692809 | C | G | 9 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0001c0003t0018g0283 others(6): Show |
9 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+9941C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692809 | |||||||
| chr7:4692811 | T | C | 1 | a0001c0003t0031g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.560+9943T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692811 | |||||||
| chr7:4692829 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.560+9961C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692829 | |||||||
| chr7:4692938 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.560+10070C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692938 | |||||||
| chr7:4692940 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0042g0139 |
2 | HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.560+10072C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692940 | |||||||
| chr7:4692953 | G | A | 4 | a0001c0002t0020g0285 a0001c0003t0062g0072 a0001c0003t0091g0278 others(1): Show |
4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+10085G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692953 | |||||||
| chr7:4692955 | T | G | 2 | a0001c0004t0003g0140 a0001c0004t0007g0141 |
2 | NA18951.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.560+10087T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4692955 | |||||||
| chr7:4693120 | G | T | 1 | a0001c0001t0006g0258 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.560+10252G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693120 | |||||||
| chr7:4693277 | A | G | 1 | a0001c0002t0033g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+10409A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693277 | |||||||
| chr7:4693387 | T | C | 1 | a0001c0009t0003g0142 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.560+10519T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693387 | |||||||
| chr7:4693443 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.560+10575A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693443 | |||||||
| chr7:4693564 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.560+10696T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693564 | |||||||
| chr7:4693582 | C | T | 2 | a0001c0003t0018g0283 a0001c0003t0025g0210 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+10714C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693582 | |||||||
| chr7:4693585 | C | T | 1 | a0001c0017t0016g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.560+10717C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693585 | |||||||
| chr7:4693927 | C | T | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.560+11059C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4693927 | |||||||
| chr7:4694286 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.560+11418T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694286 | |||||||
| chr7:4694390 | C | G | 4 | a0001c0002t0020g0285 a0001c0003t0062g0072 a0001c0003t0091g0278 others(1): Show |
4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+11522C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694390 | |||||||
| chr7:4694479 | C | T | 2 | a0001c0003t0071g0250 a0001c0004t0097g0248 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+11611C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694479 | |||||||
| chr7:4694711 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.560+11843G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694711 | |||||||
| chr7:4694828 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0040 |
3 | HG00544.hp2 NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.560+11960C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694828 | |||||||
| chr7:4694863 | T | G | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+11995T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4694863 | |||||||
| chr7:4695097 | G | A | 1 | a0001c0003t0012g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.560+12229G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695097 | |||||||
| chr7:4695216 | C | T | 4 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0059 others(1): Show |
4 | HG01074.hp2 HG03017.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+12348C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695216 | |||||||
| chr7:4695441 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+12573G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695441 | |||||||
| chr7:4695475 | G | C | 2 | a0001c0003t0002g0238 a0001c0003t0012g0229 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+12607G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695475 | |||||||
| chr7:4695498 | G | T | 24 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0002g0227 others(21): Show |
24 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.560+12630G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695498 | |||||||
| chr7:4695525 | C | T | 44 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(41): Show |
45 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.560+12657C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695525 | |||||||
| chr7:4695691 | C | G | 13 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0069g0268 others(10): Show |
14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.560+12823C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695691 | |||||||
| chr7:4695758 | G | A | 2 | a0001c0003t0071g0250 a0001c0004t0097g0248 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+12890G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695758 | |||||||
| chr7:4695843 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.560+12975G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695843 | |||||||
| chr7:4695876 | C | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0216 |
2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.560+13008C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695876 | |||||||
| chr7:4695877 | G | A | 21 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0002g0227 others(18): Show |
21 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+13009G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695877 | |||||||
| chr7:4695936 | C | CA | 112 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(109): Show |
114 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.560+13086dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4695936 | ||||||
| chr7:4695974 | G | T | 2 | a0001c0003t0012g0229 a0001c0003t0095g0073 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+13106G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695974 | |||||||
| chr7:4695985 | G | A | 1 | a0001c0004t0035g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+13117G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695985 | |||||||
| chr7:4695998 | C | T | 1 | a0001c0011t0004g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.560+13130C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4695998 | |||||||
| chr7:4696002 | A | G | 58 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(55): Show |
59 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.560+13134A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696002 | |||||||
| chr7:4696019 | G | A | 1 | a0001c0002t0060g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.560+13151G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696019 | |||||||
| chr7:4696094 | C | A | 11 | a0001c0001t0067g0094 a0001c0003t0011g0236 a0001c0003t0015g0086 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.560+13226C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696094 | |||||||
| chr7:4696115 | CA | C | 58 | a0001c0001t0001g0034 a0001c0001t0001g0121 a0001c0001t0001g0184 others(55): Show |
59 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.560+13266delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4696115 | ||||||
| chr7:4696186 | A | G | 1 | a0001c0004t0010g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.560+13318A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696186 | |||||||
| chr7:4696202 | A | T | 1 | a0001c0003t0011g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+13334A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696202 | |||||||
| chr7:4696303 | G | T | 4 | a0001c0002t0001g0222 a0001c0002t0001g0260 a0001c0002t0001g0276 others(1): Show |
4 | HG00735.hp2 HG01099.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+13435G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696303 | |||||||
| chr7:4696306 | G | A | 1 | a0001c0002t0033g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+13438G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696306 | |||||||
| chr7:4696341 | G | C | 1 | a0001c0003t0032g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+13473G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696341 | |||||||
| chr7:4696442 | G | T | 1 | a0001c0003t0025g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+13574G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696442 | |||||||
| chr7:4696496 | C | A | 1 | a0001c0002t0001g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.560+13628C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696496 | |||||||
| chr7:4696532 | G | T | 2 | a0001c0003t0071g0250 a0001c0004t0097g0248 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+13664G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696532 | |||||||
| chr7:4696573 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.560+13705G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696573 | |||||||
| chr7:4696598 | G | A | 2 | a0001c0002t0074g0237 a0001c0007t0078g0090 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560+13730G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696598 | |||||||
| chr7:4696687 | A | G | 2 | a0001c0003t0071g0250 a0001c0004t0097g0248 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+13819A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696687 | |||||||
| chr7:4696830 | G | C | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+13962G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696830 | |||||||
| chr7:4696924 | C | T | 25 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(22): Show |
25 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.560+14056C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696924 | |||||||
| chr7:4696942 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.560+14074C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696942 | |||||||
| chr7:4696960 | C | T | 3 | a0001c0002t0044g0087 a0001c0003t0070g0281 a0001c0019t0090g0219 |
3 | HG02970.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.560+14092C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4696960 | |||||||
| chr7:4697079 | A | G | 54 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(51): Show |
55 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.560+14211A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697079 | |||||||
| chr7:4697130 | G | T | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.560+14262G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697130 | |||||||
| chr7:4697145 | G | A | 1 | a0001c0002t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+14277G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697145 | |||||||
| chr7:4697267 | A | G | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+14399A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697267 | |||||||
| chr7:4697294 | A | G | 3 | a0001c0002t0044g0087 a0001c0003t0070g0281 a0001c0019t0090g0219 |
3 | HG02970.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.560+14426A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697294 | |||||||
| chr7:4697336 | G | C | 2 | a0001c0003t0012g0229 a0001c0003t0095g0073 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+14468G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697336 | |||||||
| chr7:4697343 | T | C | 2 | a0001c0001t0001g0063 a0001c0002t0001g0051 |
2 | HG01515.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.560+14475T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697343 | |||||||
| chr7:4697390 | C | G | 4 | a0001c0002t0020g0285 a0001c0003t0062g0072 a0001c0003t0091g0278 others(1): Show |
4 | HG01081.hp2 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+14522C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697390 | |||||||
| chr7:4697544 | G | A | 2 | a0001c0003t0012g0229 a0001c0003t0095g0073 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.560+14676G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697544 | |||||||
| chr7:4697605 | G | C | 54 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(51): Show |
55 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.560+14737G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697605 | |||||||
| chr7:4697685 | G | A | 1 | a0001c0004t0040g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560+14817G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697685 | |||||||
| chr7:4697696 | CTTA | C | 3 | a0001c0003t0071g0250 a0001c0004t0010g0137 a0001c0004t0097g0248 |
3 | HG03209.hp1 HG03486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.560+14834_560+1483 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697696 | ||||||
| chr7:4697729 | AG | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0003t0017g0143 others(2): Show |
6 | HG02602.hp2 HG03491.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+14863delG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697729 | ||||||
| chr7:4697741 | C | CTG | 3 | a0001c0001t0001g0119 a0001c0001t0061g0183 a0001c0002t0001g0145 |
3 | HG02135.hp1 HG02155.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.560+14921_560+1492 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTG | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(70): Show |
73 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.560+14921_560+1492 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTG | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0046 others(74): Show |
78 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.560+14919_560+1492 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTGTG | C | 42 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0054 others(39): Show |
42 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.560+14917_560+1492 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTGTGT others(1): Show |
C | 33 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0063 others(30): Show |
33 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.560+14915_560+1492 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0047g0249 a0001c0002t0001g0112 a0001c0003t0012g0229 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+14913_560+1492 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTGTGT others(5): Show |
C | 5 | a0001c0002t0001g0135 a0001c0002t0050g0134 a0001c0003t0003g0199 others(2): Show |
5 | HG02109.hp1 HG03209.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+14911_560+1492 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0181 a0001c0004t0097g0248 |
2 | HG01099.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+14909_560+1492 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTGTGT others(9): Show |
C | 14 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0069g0268 others(11): Show |
15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.560+14907_560+1492 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697741 | CTGTGTGT others(11): Show |
C | 1 | a0001c0002t0001g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.560+14905_560+1492 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697741 | ||||||
| chr7:4697785 | GTGTGT | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0138 a0001c0003t0092g0149 |
3 | HG01981.hp2 HG02698.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.560+14919_560+1492 others(9): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4697785 | ||||||
| chr7:4697821 | T | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+14953T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697821 | |||||||
| chr7:4697860 | T | C | 1 | a0001c0004t0007g0144 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.560+14992T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697860 | |||||||
| chr7:4697886 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.560+15018G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697886 | |||||||
| chr7:4697985 | T | C | 69 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(66): Show |
70 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.560+15117T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4697985 | |||||||
| chr7:4698195 | A | C | 1 | a0001c0006t0013g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.560+15327A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698195 | |||||||
| chr7:4698304 | A | ATG | 14 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0069g0268 others(11): Show |
15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.560+15444_560+1544 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698304 | ||||||
| chr7:4698312 | G | GTA | 9 | a0001c0001t0001g0054 a0001c0001t0001g0230 a0001c0001t0001g0235 others(6): Show |
9 | HG02083.hp2 HG02738.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+15462_560+1546 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | ||||||
| chr7:4698312 | G | GTGTA | 3 | a0001c0002t0074g0237 a0001c0003t0018g0283 a0001c0003t0025g0210 |
3 | HG02895.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.560+15445_560+1544 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | ||||||
| chr7:4698312 | G | GTGTATA | 3 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0002c0013t0008g0288 |
3 | HG02559.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.560+15445_560+1544 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | ||||||
| chr7:4698312 | G | GTGTATAT others(1): Show |
4 | a0001c0006t0013g0075 a0001c0006t0013g0076 a0001c0006t0013g0077 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+15445_560+1544 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4698312 | ||||||
| chr7:4698314 | A | G | 7 | a0001c0001t0001g0192 a0001c0002t0001g0160 a0001c0002t0001g0161 others(4): Show |
7 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+15446A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698314 | |||||||
| chr7:4698320 | A | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+15452A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698320 | |||||||
| chr7:4698393 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.560+15525G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698393 | |||||||
| chr7:4698822 | G | A | 1 | a0001c0004t0035g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+15954G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698822 | |||||||
| chr7:4698905 | C | G | 1 | a0001c0002t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+16037C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4698905 | |||||||
| chr7:4699041 | C | T | 1 | a0001c0002t0001g0215 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.560+16173C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699041 | |||||||
| chr7:4699129 | T | C | 1 | a0001c0007t0078g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+16261T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699129 | |||||||
| chr7:4699141 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0031 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.560+16273C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699141 | |||||||
| chr7:4699285 | GT | G | 22 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0002g0227 others(19): Show |
22 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.560+16434delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4699285 | ||||||
| chr7:4699286 | T | TTTTTTTT others(82): Show |
1 | a0001c0002t0001g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.560+16419_560+1650 others(93): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4699286 | ||||||
| chr7:4699306 | A | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+16438A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699306 | |||||||
| chr7:4699345 | C | T | 19 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0066g0209 others(16): Show |
20 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.560+16477C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699345 | |||||||
| chr7:4699376 | G | GT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): Show |
75 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.560+16521dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4699376 | ||||||
| chr7:4699429 | C | G | 26 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(23): Show |
26 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.560+16561C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699429 | |||||||
| chr7:4699492 | C | T | 1 | a0001c0001t0048g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+16624C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699492 | |||||||
| chr7:4699512 | T | C | 16 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0069g0268 others(13): Show |
17 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+16644T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699512 | |||||||
| chr7:4699584 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+16716T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699584 | |||||||
| chr7:4699616 | C | G | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+16748C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4699616 | |||||||
| chr7:4700015 | G | T | 1 | a0001c0003t0012g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.560+17147G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700015 | |||||||
| chr7:4700020 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.560+17152G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700020 | |||||||
| chr7:4700091 | G | A | 1 | a0001c0003t0008g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560+17223G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700091 | |||||||
| chr7:4700169 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.560+17301G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700169 | |||||||
| chr7:4700179 | A | G | 1 | a0001c0003t0018g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+17311A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700179 | |||||||
| chr7:4700233 | A | G | 3 | a0001c0002t0066g0209 a0001c0003t0031g0005 a0001c0003t0080g0060 |
3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+17365A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700233 | |||||||
| chr7:4700322 | T | G | 27 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(24): Show |
27 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.560+17454T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700322 | |||||||
| chr7:4700328 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.560+17460C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700328 | |||||||
| chr7:4700366 | A | G | 3 | a0001c0002t0066g0209 a0001c0003t0031g0005 a0001c0003t0080g0060 |
3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+17498A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700366 | |||||||
| chr7:4700581 | C | T | 1 | a0001c0004t0010g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560+17713C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700581 | |||||||
| chr7:4700604 | C | CCAGGTGT others(6): Show |
1 | a0001c0003t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+17738_560+1775 others(17): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4700604 | ||||||
| chr7:4700798 | C | T | 1 | a0001c0004t0010g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560+17930C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700798 | |||||||
| chr7:4700858 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0177 |
2 | NA18980.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.560+17990T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700858 | |||||||
| chr7:4700962 | G | A | 1 | a0001c0023t0041g0105 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.560+18094G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700962 | |||||||
| chr7:4700990 | A | G | 63 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(60): Show |
64 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.560+18122A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4700990 | |||||||
| chr7:4701094 | C | A | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+18226C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701094 | |||||||
| chr7:4701176 | G | A | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+18308G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701176 | |||||||
| chr7:4701189 | C | T | 1 | a0001c0003t0099g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.560+18321C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701189 | |||||||
| chr7:4701197 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.560+18329G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701197 | |||||||
| chr7:4701253 | C | CG | 8 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0034 others(5): Show |
8 | HG00408.hp2 HG02071.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+18391dupG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4701253 | ||||||
| chr7:4701303 | A | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0118 |
3 | HG02071.hp2 NA18944.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.560+18435A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701303 | |||||||
| chr7:4701394 | C | A | 1 | a0001c0002t0001g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.560+18526C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701394 | |||||||
| chr7:4701656 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0031 others(24): Show |
27 | HG00323.hp2 HG00621.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.560+18788G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701656 | |||||||
| chr7:4701698 | C | T | 1 | a0001c0003t0012g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.560+18830C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701698 | |||||||
| chr7:4701786 | G | A | 2 | a0001c0001t0020g0224 a0001c0004t0040g0186 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.560+18918G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701786 | |||||||
| chr7:4701790 | G | A | 1 | a0001c0002t0002g0282 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.560+18922G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701790 | |||||||
| chr7:4701812 | G | C | 3 | a0001c0002t0066g0209 a0001c0003t0031g0005 a0001c0003t0080g0060 |
3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+18944G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701812 | |||||||
| chr7:4701817 | T | C | 1 | a0001c0003t0018g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+18949T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701817 | |||||||
| chr7:4701818 | G | A | 1 | a0001c0003t0018g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+18950G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701818 | |||||||
| chr7:4701850 | G | A | 2 | a0001c0001t0001g0020 a0001c0003t0025g0210 |
2 | HG03579.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.560+18982G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701850 | |||||||
| chr7:4701872 | G | A | 1 | a0001c0007t0078g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+19004G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701872 | |||||||
| chr7:4701886 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0040 |
2 | NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.560+19018C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701886 | |||||||
| chr7:4701942 | G | A | 4 | a0001c0001t0001g0259 a0001c0002t0001g0195 a0001c0002t0001g0196 others(1): Show |
4 | HG02071.hp1 HG02132.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+19074G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4701942 | |||||||
| chr7:4702031 | T | C | 56 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(53): Show |
57 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.560+19163T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702031 | |||||||
| chr7:4702041 | C | G | 1 | a0001c0003t0025g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+19173C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702041 | |||||||
| chr7:4702101 | A | G | 29 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(26): Show |
29 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.560+19233A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702101 | |||||||
| chr7:4702229 | G | A | 3 | a0001c0003t0018g0283 a0001c0003t0025g0210 a0001c0003t0082g0275 |
3 | HG02895.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+19361G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702229 | |||||||
| chr7:4702285 | C | T | 2 | a0001c0001t0001g0063 a0001c0002t0001g0051 |
2 | HG01515.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.560+19417C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702285 | |||||||
| chr7:4702356 | T | A | 4 | a0001c0001t0023g0015 a0001c0001t0052g0146 a0001c0004t0003g0120 others(1): Show |
4 | HG02698.hp1 NA18962.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+19488T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702356 | |||||||
| chr7:4702360 | T | G | 9 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(6): Show |
9 | HG02572.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+19492T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702360 | |||||||
| chr7:4702373 | C | T | 1 | a0001c0003t0015g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.560+19505C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702373 | |||||||
| chr7:4702416 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.560+19548C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702416 | |||||||
| chr7:4702672 | T | A | 32 | a0001c0001t0067g0094 a0001c0002t0001g0066 a0001c0002t0002g0227 others(29): Show |
32 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.560+19804T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702672 | |||||||
| chr7:4702793 | G | A | 1 | a0001c0001t0067g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.560+19925G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702793 | |||||||
| chr7:4702821 | A | T | 3 | a0001c0002t0066g0209 a0001c0003t0031g0005 a0001c0003t0080g0060 |
3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+19953A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702821 | |||||||
| chr7:4702861 | C | T | 31 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(28): Show |
31 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.560+19993C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702861 | |||||||
| chr7:4702983 | C | T | 2 | a0001c0003t0018g0283 a0001c0003t0025g0210 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+20115C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4702983 | |||||||
| chr7:4703053 | G | T | 3 | a0001c0003t0008g0101 a0001c0003t0008g0197 a0001c0003t0073g0093 |
3 | HG02717.hp2 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.560+20185G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703053 | |||||||
| chr7:4703091 | T | C | 72 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(69): Show |
73 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.560+20223T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703091 | |||||||
| chr7:4703092 | G | A | 1 | a0001c0003t0018g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.560+20224G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703092 | |||||||
| chr7:4703179 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.560+20311G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703179 | |||||||
| chr7:4703318 | A | G | 4 | a0001c0002t0020g0285 a0001c0003t0062g0072 a0001c0003t0091g0278 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+20450A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703318 | |||||||
| chr7:4703414 | C | T | 1 | a0001c0007t0078g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+20546C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703414 | |||||||
| chr7:4703471 | C | A | 7 | a0001c0002t0074g0237 a0001c0003t0008g0262 a0001c0003t0026g0079 others(4): Show |
7 | HG02809.hp1 HG02970.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+20603C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703471 | |||||||
| chr7:4703503 | G | A | 3 | a0001c0002t0066g0209 a0001c0003t0031g0005 a0001c0003t0080g0060 |
3 | HG02818.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.560+20635G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703503 | |||||||
| chr7:4703512 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.560+20644G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703512 | |||||||
| chr7:4703690 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.560+20822G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703690 | |||||||
| chr7:4703715 | C | T | 2 | a0001c0003t0018g0283 a0001c0003t0025g0210 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+20847C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703715 | |||||||
| chr7:4703743 | C | A | 63 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(60): Show |
64 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.560+20875C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703743 | |||||||
| chr7:4703743 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.560+20875C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4703743 | |||||||
| chr7:4704084 | G | A | 4 | a0001c0002t0020g0285 a0001c0003t0062g0072 a0001c0003t0091g0278 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+21216G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704084 | |||||||
| chr7:4704311 | C | T | 1 | a0001c0007t0078g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.560+21443C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704311 | |||||||
| chr7:4704450 | C | CA | 25 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0110 others(22): Show |
25 | HG01099.hp1 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.560+21600dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704450 | ||||||
| chr7:4704450 | C | CAA | 11 | a0001c0002t0001g0107 a0001c0002t0002g0069 a0001c0002t0069g0268 others(8): Show |
12 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+21599_560+2160 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704450 | ||||||
| chr7:4704463 | A | G | 8 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0001c0006t0013g0075 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+21595A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704463 | |||||||
| chr7:4704464 | A | G | 7 | a0001c0002t0074g0237 a0001c0003t0008g0262 a0001c0003t0026g0079 others(4): Show |
7 | HG02809.hp1 HG02970.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+21596A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704464 | |||||||
| chr7:4704601 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.560+21733A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704601 | |||||||
| chr7:4704621 | C | T | 21 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0002g0227 others(18): Show |
21 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.560+21753C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704621 | |||||||
| chr7:4704676 | C | T | 34 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(31): Show |
34 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.560+21808C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704676 | |||||||
| chr7:4704690 | C | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+21822C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704690 | |||||||
| chr7:4704745 | T | C | 1 | a0001c0002t0020g0285 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560+21877T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704745 | |||||||
| chr7:4704830 | C | T | 45 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(42): Show |
45 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.560+21962C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4704830 | |||||||
| chr7:4704834 | C | CTTTTTTT others(2): Show |
6 | a0001c0002t0069g0268 a0001c0003t0018g0207 a0001c0004t0038g0010 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+21973_560+2198 others(13): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(3): Show |
8 | a0001c0002t0001g0107 a0001c0003t0001g0113 a0001c0003t0008g0074 others(5): Show |
8 | HG01070.hp1 HG01106.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+21972_560+2198 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(4): Show |
3 | a0001c0002t0001g0066 a0001c0003t0039g0082 a0001c0004t0035g0092 |
3 | HG02109.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+21971_560+2198 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(5): Show |
22 | a0001c0001t0019g0241 a0001c0002t0002g0227 a0001c0002t0002g0239 others(19): Show |
22 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.560+21970_560+2198 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(6): Show |
13 | a0001c0001t0067g0094 a0001c0002t0002g0245 a0001c0002t0046g0244 others(10): Show |
13 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.560+21969_560+2198 others(17): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0047g0249 a0001c0003t0082g0275 a0002c0012t0019g0290 |
3 | HG01109.hp1 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.560+21968_560+2198 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(8): Show |
9 | a0001c0002t0002g0282 a0001c0002t0033g0103 a0001c0003t0015g0246 others(6): Show |
9 | HG01081.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+21967_560+2198 others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(9): Show |
1 | a0001c0004t0097g0248 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+21981_560+2198 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(12): Show |
1 | a0001c0003t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+21981_560+2198 others(23): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(17): Show |
2 | a0001c0003t0031g0005 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.560+21981_560+2198 others(28): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4704834 | C | CTTTTTTT others(18): Show |
1 | a0001c0002t0066g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.560+21981_560+2198 others(29): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4704834 | ||||||
| chr7:4705165 | A | G | 4 | a0001c0002t0020g0285 a0001c0003t0062g0072 a0001c0003t0091g0278 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+22297A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705165 | |||||||
| chr7:4705313 | C | T | 1 | a0001c0002t0020g0285 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560+22445C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705313 | |||||||
| chr7:4705511 | TTCTCTTT others(3): Show |
T | 2 | a0001c0003t0018g0283 a0002c0012t0019g0290 |
2 | HG01109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705511 | ||||||
| chr7:4705513 | CTCTT | C | 3 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0002c0013t0015g0287 |
3 | HG01496.hp1 HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705513 | ||||||
| chr7:4705515 | CT | C | 4 | a0001c0001t0001g0202 a0001c0001t0022g0220 a0001c0002t0001g0047 others(1): Show |
4 | HG01123.hp1 HG04228.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+22650delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705515 | ||||||
| chr7:4705516 | TTTCTCTC others(4): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.560+22650_560+2266 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705516 | ||||||
| chr7:4705517 | T | C | 18 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(15): Show |
19 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.560+22649T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | |||||||
| chr7:4705517 | T | TC | 5 | a0001c0001t0001g0054 a0001c0001t0001g0235 a0001c0002t0001g0009 others(2): Show |
5 | HG02083.hp2 HG02738.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22649_560+2265 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | |||||||
| chr7:4705517 | T | TCTC | 6 | a0001c0001t0001g0046 a0001c0001t0058g0064 a0001c0002t0036g0156 others(3): Show |
6 | HG00738.hp1 HG02074.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+22649_560+2265 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | |||||||
| chr7:4705517 | T | TCTCTC | 3 | a0001c0002t0001g0257 a0001c0007t0004g0085 a0001c0009t0003g0142 |
3 | HG01433.hp2 HG02145.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(9): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | |||||||
| chr7:4705517 | T | TCTCTCTC others(4): Show |
3 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0072g0208 |
3 | HG02717.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.560+22649_560+2265 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705517 | |||||||
| chr7:4705517 | T | TTC | 37 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0043 others(34): Show |
37 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+22690_560+2269 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | T | TTCTC | 22 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0051g0025 others(19): Show |
22 | HG01891.hp1 HG01928.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.560+22688_560+2269 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | T | TTCTCTC | 15 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0110 others(12): Show |
15 | HG00621.hp1 HG01192.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.560+22686_560+2269 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | T | TTCTCTCT others(1): Show |
16 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
16 | HG02155.hp2 HG02523.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.560+22684_560+2269 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | T | TTCTCTCT others(3): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0177 a0001c0001t0001g0265 others(3): Show |
6 | HG01346.hp2 HG02004.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+22682_560+2269 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | T | TTCTCTCT others(5): Show |
2 | a0001c0001t0049g0039 a0001c0002t0002g0068 |
2 | HG02056.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.560+22680_560+2269 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | T | TTCTCTCT others(7): Show |
4 | a0001c0002t0001g0191 a0001c0002t0006g0194 a0001c0003t0005g0242 others(1): Show |
4 | HG02132.hp2 HG02165.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+22678_560+2269 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | T | TTCTCTCT others(11): Show |
1 | a0001c0001t0001g0259 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.560+22674_560+2269 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | TTC | T | 40 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0036 others(37): Show |
41 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.560+22690_560+2269 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | TTCTC | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0185 a0001c0002t0001g0135 others(3): Show |
6 | HG00558.hp2 HG01361.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+22688_560+2269 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | TTCTCTCT others(5): Show |
T | 1 | a0001c0002t0002g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.560+22680_560+2269 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705517 | TTCTCTCT others(7): Show |
T | 9 | a0001c0001t0019g0241 a0001c0002t0002g0227 a0001c0002t0002g0239 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+22678_560+2269 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705517 | ||||||
| chr7:4705525 | C | T | 1 | a0001c0010t0079g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.560+22657C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705525 | |||||||
| chr7:4705534 | T | TCTCTCGC others(11): Show |
1 | a0001c0003t0012g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+22671_560+2267 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705534 | ||||||
| chr7:4705540 | T | G | 1 | a0001c0003t0012g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.560+22672T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705540 | |||||||
| chr7:4705540 | T | TCTCTCGC others(5): Show |
1 | a0001c0003t0031g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.560+22677_560+2267 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705540 | ||||||
| chr7:4705546 | T | G | 4 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0031g0005 others(1): Show |
4 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+22678T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705546 | |||||||
| chr7:4705546 | T | TCGCTCTC others(7): Show |
1 | a0001c0003t0018g0207 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.560+22679_560+2268 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | ||||||
| chr7:4705546 | T | TCTCGCTC others(9): Show |
1 | a0001c0021t0016g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.560+22681_560+2268 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | ||||||
| chr7:4705546 | T | TCTCTCGC others(5): Show |
2 | a0001c0004t0038g0010 a0001c0011t0004g0280 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.560+22683_560+2268 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | ||||||
| chr7:4705546 | T | TCTCTCGC others(11): Show |
5 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(2): Show |
5 | HG01433.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22683_560+2268 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705546 | ||||||
| chr7:4705552 | T | G | 14 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(11): Show |
14 | HG01261.hp1 HG01433.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.560+22684T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705552 | |||||||
| chr7:4705552 | T | TCGCTCTC others(7): Show |
1 | a0001c0004t0001g0114 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.560+22685_560+2268 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | ||||||
| chr7:4705552 | T | TCGCTCTC others(13): Show |
1 | a0001c0003t0012g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.560+22685_560+2268 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | ||||||
| chr7:4705552 | T | TCTCGCTC others(9): Show |
1 | a0001c0003t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.560+22687_560+2268 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | ||||||
| chr7:4705552 | T | TCTCGCTC others(15): Show |
1 | a0001c0006t0009g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.560+22687_560+2268 others(26): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705552 | ||||||
| chr7:4705554 | T | TCGCTCTC others(1): Show |
7 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+22687_560+2268 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | ||||||
| chr7:4705554 | T | TCTCGCTC others(3): Show |
1 | a0001c0011t0004g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.560+22689_560+2269 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | ||||||
| chr7:4705554 | T | TCTCTCG | 30 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0002g0227 others(27): Show |
30 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.560+22698_560+2270 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | ||||||
| chr7:4705554 | T | TCTCTCGC others(5): Show |
5 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0001c0003t0039g0082 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22692_560+2270 others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | ||||||
| chr7:4705554 | T | TCTCTCGC others(11): Show |
3 | a0001c0003t0018g0283 a0001c0003t0025g0210 a0002c0012t0019g0290 |
3 | HG01109.hp1 HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.560+22703_560+2270 others(22): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | ||||||
| chr7:4705554 | T | TCTCTCTC others(13): Show |
1 | a0001c0002t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560+22691_560+2269 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705554 | ||||||
| chr7:4705556 | T | G | 1 | a0001c0004t0003g0032 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.560+22688T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705556 | |||||||
| chr7:4705556 | TCTCG | T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0184 a0001c0001t0006g0258 others(2): Show |
5 | HG00558.hp1 HG02074.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+22692_560+2269 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705556 | ||||||
| chr7:4705558 | TCG | T | 4 | a0001c0001t0001g0162 a0001c0004t0003g0140 a0001c0004t0007g0141 others(1): Show |
4 | HG04115.hp2 NA18951.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+22692_560+2269 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705558 | ||||||
| chr7:4705560 | G | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.560+22692G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705560 | |||||||
| chr7:4705587 | A | G | 2 | a0001c0001t0001g0013 a0001c0002t0023g0048 |
2 | HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.560+22719A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705587 | |||||||
| chr7:4705588 | G | A | 18 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(15): Show |
19 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.560+22720G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705588 | |||||||
| chr7:4705629 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0034 others(5): Show |
8 | HG00408.hp2 HG02071.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+22761C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705629 | |||||||
| chr7:4705656 | C | G | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.560+22788C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705656 | |||||||
| chr7:4705688 | G | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+22820G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705688 | |||||||
| chr7:4705689 | C | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+22821C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705689 | |||||||
| chr7:4705767 | A | G | 70 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(67): Show |
71 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.560+22899A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705767 | |||||||
| chr7:4705776 | A | AC | 39 | a0001c0001t0001g0115 a0001c0001t0001g0147 a0001c0001t0001g0259 others(36): Show |
40 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.560+22917dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705776 | ||||||
| chr7:4705778 | C | CA | 9 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(6): Show |
9 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+22910_560+2291 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705778 | |||||||
| chr7:4705780 | C | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0221 a0001c0008t0003g0206 |
3 | HG02129.hp2 NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.560+22912C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705780 | |||||||
| chr7:4705783 | C | CG | 3 | a0001c0003t0039g0082 a0001c0004t0011g0255 a0001c0004t0035g0092 |
3 | HG02109.hp1 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.560+22915_560+2291 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705783 | |||||||
| chr7:4705792 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0221 a0001c0008t0003g0206 |
3 | HG02129.hp2 NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.560+22924G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705792 | |||||||
| chr7:4705959 | T | C | 7 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0001c0003t0008g0262 others(4): Show |
7 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+23091T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705959 | |||||||
| chr7:4705959 | T | TGTATATA others(37): Show |
1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.560+23101_560+2314 others(48): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705959 | ||||||
| chr7:4705960 | GTA | G | 37 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0001g0066 others(34): Show |
37 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+23103_560+2310 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705960 | ||||||
| chr7:4705960 | GTATATAT others(39): Show |
G | 6 | a0001c0001t0001g0192 a0001c0002t0001g0160 a0001c0002t0001g0161 others(3): Show |
6 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+23099_560+2314 others(50): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705960 | ||||||
| chr7:4705962 | A | G | 1 | a0001c0004t0040g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560+23094A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705962 | |||||||
| chr7:4705962 | ATATATAT others(35): Show |
A | 8 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+23103_560+2314 others(46): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705962 | ||||||
| chr7:4705964 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0163 a0001c0002t0020g0285 |
2 | HG03669.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.560+23148_560+2315 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | ||||||
| chr7:4705964 | A | ATATATAT others(13): Show |
5 | a0001c0001t0030g0065 a0001c0002t0002g0252 a0001c0003t0005g0091 others(2): Show |
5 | HG00673.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+23138_560+2315 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | ||||||
| chr7:4705964 | A | ATATATAT others(43): Show |
1 | a0001c0002t0002g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.560+23108_560+2315 others(54): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | ||||||
| chr7:4705964 | ATATATAT others(3): Show |
A | 25 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0043 others(22): Show |
26 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.560+23148_560+2315 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | ||||||
| chr7:4705964 | ATATATAT others(13): Show |
A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0121 a0001c0001t0001g0155 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+23138_560+2315 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | ||||||
| chr7:4705964 | ATATATAT others(23): Show |
A | 2 | a0004c0016t0075g0150 a0004c0016t0076g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.560+23128_560+2315 others(34): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | ||||||
| chr7:4705964 | ATATATAT others(33): Show |
A | 3 | a0001c0002t0001g0132 a0001c0002t0001g0133 a0001c0003t0086g0213 |
3 | HG01256.hp1 HG01258.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.560+23118_560+2315 others(44): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705964 | ||||||
| chr7:4705970 | A | ATG | 3 | a0001c0002t0001g0107 a0001c0002t0069g0268 a0001c0006t0009g0002 |
4 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23103_560+2310 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705970 | ||||||
| chr7:4705970 | A | ATGTATAT others(39): Show |
1 | a0001c0007t0004g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.560+23103_560+2310 others(50): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705970 | ||||||
| chr7:4705971 | T | C | 2 | a0001c0001t0064g0045 a0005c0025t0014g0033 |
2 | HG00621.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.560+23103T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705971 | |||||||
| chr7:4705972 | A | G | 12 | a0001c0002t0066g0209 a0001c0003t0002g0238 a0001c0003t0012g0067 others(9): Show |
12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23104A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705972 | |||||||
| chr7:4705973 | C | T | 15 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23105C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705973 | |||||||
| chr7:4705974 | G | A | 15 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23106G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705974 | |||||||
| chr7:4705974 | GTATATAT others(25): Show |
G | 1 | a0001c0008t0087g0271 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.560+23113_560+2314 others(36): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705974 | ||||||
| chr7:4705981 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0201 |
2 | HG00597.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.560+23113T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705981 | |||||||
| chr7:4705983 | C | CATATATA others(45): Show |
3 | a0001c0002t0001g0107 a0001c0002t0069g0268 a0001c0006t0009g0002 |
4 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23115_560+2311 others(56): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705983 | |||||||
| chr7:4705983 | C | T | 12 | a0001c0002t0066g0209 a0001c0003t0002g0238 a0001c0003t0012g0067 others(9): Show |
12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23115C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705983 | |||||||
| chr7:4705984 | G | A | 12 | a0001c0002t0066g0209 a0001c0003t0002g0238 a0001c0003t0012g0067 others(9): Show |
12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23116G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705984 | |||||||
| chr7:4705984 | G | GTATATAT others(45): Show |
1 | a0001c0002t0046g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.560+23124_560+2312 others(56): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705984 | ||||||
| chr7:4705984 | G | GTATATAT others(69): Show |
1 | a0001c0002t0033g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560+23124_560+2312 others(80): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705984 | ||||||
| chr7:4705985 | T | C | 12 | a0001c0002t0066g0209 a0001c0003t0002g0238 a0001c0003t0012g0067 others(9): Show |
12 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23117T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705985 | |||||||
| chr7:4705988 | ATATACGT others(51): Show |
A | 5 | a0001c0002t0074g0237 a0001c0003t0071g0250 a0001c0003t0082g0275 others(2): Show |
5 | HG03209.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23125_560+2318 others(62): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705988 | ||||||
| chr7:4705990 | ATACGTAT others(49): Show |
A | 5 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23125_560+2318 others(60): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705990 | ||||||
| chr7:4705992 | ACG | A | 3 | a0001c0002t0001g0066 a0001c0004t0011g0255 a0001c0004t0035g0092 |
3 | HG02615.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+23125_560+2312 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705992 | |||||||
| chr7:4705993 | C | T | 15 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23125C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705993 | |||||||
| chr7:4705993 | CGTATATA others(51): Show |
C | 23 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0002g0227 others(20): Show |
23 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.560+23126_560+2318 others(62): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705993 | |||||||
| chr7:4705994 | G | A | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+23126G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705994 | |||||||
| chr7:4705994 | G | GTATGTA | 4 | a0001c0002t0001g0107 a0001c0002t0069g0268 a0001c0006t0009g0002 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23129_560+2313 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705994 | ||||||
| chr7:4705996 | A | ATATATAC others(23): Show |
2 | a0001c0001t0001g0070 a0001c0003t0062g0072 |
2 | HG02622.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.560+23138_560+2316 others(34): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4705996 | ||||||
| chr7:4705998 | A | G | 3 | a0001c0002t0001g0066 a0001c0004t0011g0255 a0001c0004t0035g0092 |
3 | HG02615.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+23130A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4705998 | |||||||
| chr7:4706001 | T | C | 1 | a0001c0005t0001g0154 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.560+23133T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706001 | |||||||
| chr7:4706002 | A | T | 3 | a0001c0001t0001g0003 a0001c0001t0022g0003 a0001c0001t0022g0220 |
3 | NA18980.hp1 NA19060.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.560+23134A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706002 | |||||||
| chr7:4706002 | ACGTATAT others(17): Show |
A | 3 | a0001c0002t0001g0066 a0001c0004t0011g0255 a0001c0004t0035g0092 |
3 | HG02615.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.560+23135_560+2315 others(28): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706002 | |||||||
| chr7:4706003 | C | T | 9 | a0001c0002t0066g0209 a0001c0003t0002g0238 a0001c0003t0012g0067 others(6): Show |
9 | HG02257.hp1 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.560+23135C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706003 | |||||||
| chr7:4706004 | G | GTATATAT others(87): Show |
1 | a0001c0021t0016g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.560+23144_560+2314 others(98): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706004 | ||||||
| chr7:4706004 | G | GTATGTA | 4 | a0001c0002t0066g0209 a0001c0003t0002g0238 a0001c0003t0031g0005 others(1): Show |
4 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23139_560+2314 others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706004 | ||||||
| chr7:4706006 | A | ATATATAC others(13): Show |
8 | a0001c0001t0001g0046 a0001c0001t0001g0111 a0001c0001t0001g0121 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+23148_560+2316 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706006 | ||||||
| chr7:4706006 | A | G | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+23138A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706006 | |||||||
| chr7:4706013 | C | T | 5 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0012g0229 others(2): Show |
5 | HG02257.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23145C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706013 | |||||||
| chr7:4706013 | CGT | C | 4 | a0001c0002t0001g0107 a0001c0002t0069g0268 a0001c0006t0009g0002 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23146_560+2314 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706013 | |||||||
| chr7:4706015 | T | TATATATA others(93): Show |
4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0018g0207 others(1): Show |
4 | HG02257.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+23154_560+2315 others(104): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706015 | ||||||
| chr7:4706015 | T | TATATATA others(49): Show |
1 | a0001c0003t0012g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.560+23154_560+2315 others(60): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706015 | ||||||
| chr7:4706016 | A | ATATATAC others(3): Show |
1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+23175_560+2318 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706016 | ||||||
| chr7:4706016 | ATATATAC others(13): Show |
A | 17 | a0001c0001t0001g0192 a0001c0002t0001g0132 a0001c0002t0001g0133 others(14): Show |
17 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23165_560+2318 others(24): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706016 | ||||||
| chr7:4706023 | C | CATATATA others(1): Show |
5 | a0001c0002t0066g0209 a0001c0003t0002g0238 a0001c0003t0031g0005 others(2): Show |
5 | HG01261.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+23155_560+2315 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706023 | |||||||
| chr7:4706023 | C | CATATATA others(45): Show |
2 | a0001c0004t0038g0010 a0001c0011t0004g0280 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.560+23155_560+2315 others(56): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706023 | |||||||
| chr7:4706023 | C | T | 9 | a0001c0002t0001g0107 a0001c0002t0069g0268 a0001c0003t0012g0067 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.560+23155C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706023 | |||||||
| chr7:4706026 | G | A | 12 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+23158G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706026 | |||||||
| chr7:4706033 | C | CGTATATA others(23): Show |
4 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0002c0012t0019g0290 others(1): Show |
4 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+23167_560+2316 others(34): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706033 | ||||||
| chr7:4706033 | C | T | 26 | a0001c0001t0047g0249 a0001c0002t0001g0107 a0001c0002t0002g0282 others(23): Show |
27 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.560+23165C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706033 | |||||||
| chr7:4706034 | G | A | 8 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+23166G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706034 | |||||||
| chr7:4706036 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(220): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.560+23168G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706036 | |||||||
| chr7:4706036 | G | GTATATAC others(3): Show |
1 | a0001c0003t0008g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560+23177_560+2317 others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706036 | ||||||
| chr7:4706043 | C | T | 24 | a0001c0001t0047g0249 a0001c0002t0001g0107 a0001c0002t0002g0282 others(21): Show |
25 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.560+23175C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706043 | |||||||
| chr7:4706044 | G | A | 8 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+23176G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706044 | |||||||
| chr7:4706046 | G | A | 26 | a0001c0002t0001g0066 a0001c0002t0001g0107 a0001c0002t0033g0103 others(23): Show |
27 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.560+23178G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706046 | |||||||
| chr7:4706053 | T | C | 11 | a0001c0001t0001g0062 a0001c0001t0001g0190 a0001c0001t0030g0065 others(8): Show |
11 | HG00673.hp2 HG01109.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.560+23185T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706053 | |||||||
| chr7:4706054 | G | A | 15 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0003t0002g0238 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+23186G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706054 | |||||||
| chr7:4706056 | A | G | 16 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23188A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706056 | |||||||
| chr7:4706062 | ATG | A | 45 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(42): Show |
45 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.560+23198_560+2319 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4706062 | ||||||
| chr7:4706064 | G | A | 16 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23196G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706064 | |||||||
| chr7:4706065 | T | C | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+23197T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706065 | |||||||
| chr7:4706204 | A | G | 16 | a0001c0002t0001g0107 a0001c0002t0066g0209 a0001c0002t0069g0268 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.560+23336A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706204 | |||||||
| chr7:4706343 | G | A | 2 | a0001c0004t0011g0255 a0001c0004t0035g0092 |
2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.560+23475G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706343 | |||||||
| chr7:4706366 | TTAG | T | 10 | a0001c0001t0019g0241 a0001c0002t0002g0227 a0001c0002t0002g0239 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+23499_560+2350 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706366 | |||||||
| chr7:4706367 | T | G | 36 | a0001c0001t0047g0249 a0001c0001t0067g0094 a0001c0002t0001g0066 others(33): Show |
36 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.560+23499T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706367 | |||||||
| chr7:4706473 | T | C | 61 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(58): Show |
62 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.560+23605T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706473 | |||||||
| chr7:4706883 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.560+24015C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706883 | |||||||
| chr7:4706908 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0004t0028g0028 others(1): Show |
4 | HG00738.hp2 HG01361.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+24040C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706908 | |||||||
| chr7:4706916 | T | A | 1 | a0001c0007t0004g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.560+24048T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706916 | |||||||
| chr7:4706981 | G | C | 64 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(61): Show |
65 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.560+24113G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4706981 | |||||||
| chr7:4707120 | C | T | 41 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(38): Show |
41 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.560+24252C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707120 | |||||||
| chr7:4707238 | G | A | 2 | a0001c0002t0001g0112 a0001c0002t0002g0282 |
2 | HG03688.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.560+24370G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707238 | |||||||
| chr7:4707414 | A | C | 3 | a0001c0003t0018g0283 a0001c0003t0025g0210 a0001c0007t0078g0090 |
3 | HG02895.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.560+24546A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707414 | |||||||
| chr7:4707506 | G | T | 6 | a0001c0002t0074g0237 a0001c0003t0008g0262 a0001c0003t0026g0079 others(3): Show |
6 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+24638G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707506 | |||||||
| chr7:4707573 | C | G | 8 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+24705C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707573 | |||||||
| chr7:4707586 | G | C | 1 | a0001c0003t0017g0157 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.560+24718G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707586 | |||||||
| chr7:4707598 | A | G | 8 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+24730A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707598 | |||||||
| chr7:4707643 | G | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+24775G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707643 | |||||||
| chr7:4707649 | C | G | 4 | a0001c0002t0074g0237 a0001c0003t0008g0262 a0001c0003t0026g0079 others(1): Show |
4 | HG02809.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+24781C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707649 | |||||||
| chr7:4707689 | C | CT | 64 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0001t0067g0094 others(61): Show |
65 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.560+24834dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4707689 | ||||||
| chr7:4707717 | C | G | 3 | a0001c0003t0071g0250 a0001c0003t0082g0275 a0001c0004t0097g0248 |
3 | HG03209.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.560+24849C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707717 | |||||||
| chr7:4707717 | C | T | 32 | a0001c0001t0019g0241 a0001c0001t0067g0094 a0001c0002t0002g0227 others(29): Show |
32 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.560+24849C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707717 | |||||||
| chr7:4707720 | C | T | 2 | a0001c0003t0025g0210 a0001c0007t0078g0090 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.560+24852C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707720 | |||||||
| chr7:4707765 | A | G | 18 | a0001c0002t0001g0066 a0001c0002t0001g0107 a0001c0002t0066g0209 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.560+24897A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707765 | |||||||
| chr7:4707954 | A | T | 8 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0003t0015g0246 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+25086A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707954 | |||||||
| chr7:4707984 | G | T | 9 | a0001c0002t0001g0107 a0001c0002t0069g0268 a0001c0003t0012g0067 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.560+25116G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4707984 | |||||||
| chr7:4708075 | T | TGGAA | 8 | a0001c0002t0001g0066 a0001c0002t0066g0209 a0001c0003t0002g0238 others(5): Show |
8 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+25211_560+2521 others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4708075 | ||||||
| chr7:4708116 | C | T | 1 | a0001c0002t0001g0170 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.560+25248C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708116 | |||||||
| chr7:4708413 | A | T | 15 | a0001c0002t0001g0107 a0001c0002t0033g0103 a0001c0002t0046g0244 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+25545A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708413 | |||||||
| chr7:4708452 | T | C | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.560+25584T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708452 | |||||||
| chr7:4708611 | G | T | 8 | a0001c0001t0001g0130 a0001c0001t0054g0129 a0001c0002t0001g0131 others(5): Show |
8 | HG00140.hp1 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+25743G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708611 | |||||||
| chr7:4708659 | A | G | 57 | a0001c0001t0019g0241 a0001c0001t0023g0015 a0001c0001t0047g0249 others(54): Show |
58 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.560+25791A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708659 | |||||||
| chr7:4708694 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.560+25826C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708694 | |||||||
| chr7:4708719 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.560+25851C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708719 | |||||||
| chr7:4708779 | G | T | 1 | a0001c0001t0048g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560+25911G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708779 | |||||||
| chr7:4708802 | C | T | 1 | a0001c0005t0014g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.560+25934C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708802 | |||||||
| chr7:4708835 | C | T | 7 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0001c0006t0013g0075 others(4): Show |
7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+25967C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708835 | |||||||
| chr7:4708874 | G | C | 30 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(27): Show |
31 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.560+26006G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708874 | |||||||
| chr7:4708958 | G | A | 2 | a0001c0001t0052g0146 a0001c0004t0007g0233 |
2 | NA19058.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.560+26090G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4708958 | |||||||
| chr7:4709020 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.560+26152G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709020 | |||||||
| chr7:4709055 | C | T | 7 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+26187C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709055 | |||||||
| chr7:4709063 | C | CA | 39 | a0001c0001t0001g0038 a0001c0001t0023g0015 a0001c0001t0047g0249 others(36): Show |
40 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.560+26211dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4709063 | ||||||
| chr7:4709075 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.560+26207A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709075 | |||||||
| chr7:4709198 | C | T | 6 | a0001c0002t0074g0237 a0001c0003t0008g0262 a0001c0003t0026g0079 others(3): Show |
6 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+26330C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709198 | |||||||
| chr7:4709199 | C | T | 6 | a0001c0002t0074g0237 a0001c0003t0008g0262 a0001c0003t0026g0079 others(3): Show |
6 | HG02809.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+26331C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709199 | |||||||
| chr7:4709203 | G | A | 1 | a0001c0027t0001g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.560+26335G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709203 | |||||||
| chr7:4709231 | G | GCATCCCC others(7): Show |
1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.560+26370_560+2638 others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4709231 | ||||||
| chr7:4709278 | T | C | 40 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(37): Show |
41 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.560+26410T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709278 | |||||||
| chr7:4709318 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.560+26450C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709318 | |||||||
| chr7:4709347 | C | T | 1 | a0001c0003t0017g0143 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.560+26479C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709347 | |||||||
| chr7:4709705 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0118 |
3 | HG02071.hp2 NA18944.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.560+26837G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709705 | |||||||
| chr7:4709726 | G | A | 15 | a0001c0001t0023g0015 a0001c0002t0001g0047 a0001c0002t0001g0107 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.560+26858G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709726 | |||||||
| chr7:4709777 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.560+26909G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709777 | |||||||
| chr7:4709788 | C | G | 32 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(29): Show |
33 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.560+26920C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709788 | |||||||
| chr7:4709896 | C | T | 26 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(23): Show |
27 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.560+27028C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709896 | |||||||
| chr7:4709897 | G | A | 1 | a0001c0003t0025g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+27029G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709897 | |||||||
| chr7:4709924 | G | T | 1 | a0001c0003t0025g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560+27056G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4709924 | |||||||
| chr7:4710047 | C | T | 2 | a0001c0002t0069g0268 a0001c0006t0009g0002 |
3 | HG01070.hp2 HG01071.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.560+27179C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710047 | |||||||
| chr7:4710468 | C | T | 20 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(17): Show |
21 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.560+27600C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710468 | |||||||
| chr7:4710527 | A | G | 7 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0001c0006t0013g0075 others(4): Show |
7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+27659A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710527 | |||||||
| chr7:4710529 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.560+27661C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710529 | |||||||
| chr7:4710718 | G | T | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+27850G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710718 | |||||||
| chr7:4710727 | C | T | 2 | a0001c0003t0099g0176 a0001c0004t0045g0232 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.560+27859C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710727 | |||||||
| chr7:4710776 | C | T | 4 | a0001c0003t0062g0072 a0001c0003t0091g0278 a0001c0003t0095g0073 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+27908C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710776 | |||||||
| chr7:4710787 | A | G | 52 | a0001c0001t0001g0020 a0001c0001t0001g0096 a0001c0001t0001g0097 others(49): Show |
53 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.560+27919A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710787 | |||||||
| chr7:4710854 | C | T | 12 | a0001c0001t0047g0249 a0001c0002t0002g0069 a0001c0002t0002g0282 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+27986C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710854 | |||||||
| chr7:4710961 | G | A | 3 | a0001c0003t0017g0143 a0001c0003t0017g0173 a0001c0003t0098g0174 |
3 | HG01081.hp1 HG01361.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.560+28093G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4710961 | |||||||
| chr7:4711038 | TTTAGAGA others(4): Show |
T | 5 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0001c0003t0002g0238 others(2): Show |
5 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+28179_560+2818 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4711038 | ||||||
| chr7:4711134 | ACTT | A | 12 | a0001c0002t0002g0227 a0001c0002t0002g0240 a0001c0002t0002g0243 others(9): Show |
12 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.560+28272_560+2827 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4711134 | ||||||
| chr7:4711159 | C | T | 8 | a0001c0002t0002g0282 a0001c0003t0015g0246 a0001c0003t0025g0210 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.560+28291C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711159 | |||||||
| chr7:4711178 | C | T | 2 | a0001c0003t0025g0254 a0001c0004t0035g0092 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.560+28310C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711178 | |||||||
| chr7:4711199 | T | G | 92 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0054 others(89): Show |
93 | HG00558.hp2 HG00735.hp2 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.560+28331T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711199 | |||||||
| chr7:4711256 | T | G | 97 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0063 others(94): Show |
98 | HG00140.hp2 HG00558.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.560+28388T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711256 | |||||||
| chr7:4711276 | G | C | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560+28408G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711276 | |||||||
| chr7:4711358 | T | A | 1 | a0003c0014t0001g0171 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.560+28490T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711358 | |||||||
| chr7:4711408 | T | C | 1 | a0001c0001t0056g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.560+28540T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711408 | |||||||
| chr7:4711490 | C | T | 1 | a0001c0002t0001g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.560+28622C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711490 | |||||||
| chr7:4711527 | C | T | 1 | a0001c0004t0029g0029 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.560+28659C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711527 | |||||||
| chr7:4711528 | C | T | 5 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+28660C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711528 | |||||||
| chr7:4711620 | G | A | 10 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+28752G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711620 | |||||||
| chr7:4711656 | T | C | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+28788T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711656 | |||||||
| chr7:4711812 | G | A | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.560+28944G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711812 | |||||||
| chr7:4711833 | T | G | 1 | a0001c0002t0066g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.560+28965T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711833 | |||||||
| chr7:4711840 | G | A | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.560+28972G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711840 | |||||||
| chr7:4711844 | G | A | 2 | a0001c0002t0044g0087 a0001c0003t0071g0250 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.560+28976G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711844 | |||||||
| chr7:4711851 | A | C | 1 | a0001c0001t0001g0020 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.560+28983A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711851 | |||||||
| chr7:4711893 | T | C | 3 | a0001c0002t0001g0135 a0001c0002t0001g0277 a0001c0002t0050g0134 |
3 | HG02738.hp1 HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.561-28945T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711893 | |||||||
| chr7:4711910 | A | C | 6 | a0001c0002t0001g0257 a0001c0003t0017g0143 a0001c0003t0017g0173 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-28928A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711910 | |||||||
| chr7:4711913 | G | A | 12 | a0001c0002t0074g0237 a0001c0003t0005g0247 a0001c0003t0011g0081 others(9): Show |
12 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-28925G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711913 | |||||||
| chr7:4711918 | G | T | 12 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(9): Show |
12 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-28920G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711918 | |||||||
| chr7:4711935 | G | A | 7 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0025g0210 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-28903G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4711935 | |||||||
| chr7:4712034 | T | C | 1 | a0001c0004t0001g0114 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561-28804T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712034 | |||||||
| chr7:4712055 | C | CT | 14 | a0001c0002t0001g0107 a0001c0002t0002g0227 a0001c0002t0002g0239 others(11): Show |
14 | HG01433.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.561-28771dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4712055 | ||||||
| chr7:4712202 | C | T | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-28636C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712202 | |||||||
| chr7:4712209 | C | T | 107 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(104): Show |
108 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(105): Show |
intron_variant | MODIFIER | c.561-28629C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712209 | |||||||
| chr7:4712388 | G | A | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-28450G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712388 | |||||||
| chr7:4712397 | A | G | 1 | a0001c0002t0001g0148 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.561-28441A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712397 | |||||||
| chr7:4712401 | A | C | 12 | a0001c0001t0001g0054 a0001c0001t0001g0096 a0001c0001t0001g0097 others(9): Show |
12 | HG00558.hp2 HG00597.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-28437A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712401 | |||||||
| chr7:4712543 | C | T | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-28295C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712543 | |||||||
| chr7:4712813 | G | A | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.561-28025G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712813 | |||||||
| chr7:4712981 | T | C | 2 | a0001c0002t0001g0132 a0001c0002t0001g0133 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.561-27857T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4712981 | |||||||
| chr7:4713004 | G | A | 102 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(99): Show |
103 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(100): Show |
intron_variant | MODIFIER | c.561-27834G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713004 | |||||||
| chr7:4713009 | A | G | 108 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(105): Show |
109 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.561-27829A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713009 | |||||||
| chr7:4713062 | T | C | 1 | a0001c0002t0006g0194 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.561-27776T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713062 | |||||||
| chr7:4713130 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.561-27708C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713130 | |||||||
| chr7:4713141 | C | T | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-27697C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713141 | |||||||
| chr7:4713163 | C | G | 1 | a0001c0001t0047g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.561-27675C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713163 | |||||||
| chr7:4713182 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.561-27656A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713182 | |||||||
| chr7:4713202 | A | C | 11 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-27636A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713202 | |||||||
| chr7:4713298 | G | A | 1 | a0001c0001t0067g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561-27540G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713298 | |||||||
| chr7:4713329 | A | AGATTCCC others(9): Show |
1 | a0001c0003t0031g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.561-27491_561-2747 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713329 | ||||||
| chr7:4713334 | C | CCCGCTCA others(9): Show |
14 | a0001c0002t0074g0237 a0001c0003t0005g0247 a0001c0003t0011g0081 others(11): Show |
14 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.561-27489_561-2748 others(20): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713334 | ||||||
| chr7:4713359 | T | C | 11 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-27479T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713359 | |||||||
| chr7:4713382 | C | T | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-27456C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713382 | |||||||
| chr7:4713434 | G | A | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-27404G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713434 | |||||||
| chr7:4713488 | GT | G | 96 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(93): Show |
97 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.561-27339delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713488 | ||||||
| chr7:4713490 | T | G | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-27348T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713490 | |||||||
| chr7:4713499 | T | G | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.561-27339T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713499 | |||||||
| chr7:4713500 | G | GT | 9 | a0001c0002t0001g0009 a0001c0002t0002g0282 a0001c0002t0033g0103 others(6): Show |
9 | HG01081.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-27328dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4713500 | ||||||
| chr7:4713500 | G | T | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.561-27338G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713500 | |||||||
| chr7:4713615 | C | T | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-27223C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713615 | |||||||
| chr7:4713736 | C | T | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-27102C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713736 | |||||||
| chr7:4713737 | G | A | 4 | a0001c0001t0047g0249 a0001c0002t0066g0209 a0001c0003t0002g0238 others(1): Show |
4 | HG02622.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-27101G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713737 | |||||||
| chr7:4713788 | C | T | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-27050C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713788 | |||||||
| chr7:4713791 | C | T | 9 | a0001c0001t0001g0192 a0001c0002t0001g0160 a0001c0002t0001g0161 others(6): Show |
9 | HG00639.hp1 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-27047C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713791 | |||||||
| chr7:4713824 | T | C | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-27014T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713824 | |||||||
| chr7:4713919 | G | A | 1 | a0001c0003t0080g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.561-26919G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4713919 | |||||||
| chr7:4714059 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.561-26779C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714059 | |||||||
| chr7:4714105 | T | G | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-26733T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714105 | |||||||
| chr7:4714106 | G | T | 5 | a0001c0001t0019g0241 a0001c0003t0099g0176 a0001c0004t0011g0255 others(2): Show |
5 | HG02615.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-26732G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714106 | |||||||
| chr7:4714276 | C | G | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-26562C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714276 | |||||||
| chr7:4714284 | G | T | 1 | a0001c0022t0001g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.561-26554G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714284 | |||||||
| chr7:4714335 | A | G | 4 | a0001c0001t0047g0249 a0001c0002t0066g0209 a0001c0003t0002g0238 others(1): Show |
4 | HG02622.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-26503A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714335 | |||||||
| chr7:4714484 | A | C | 7 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0025g0210 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-26354A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714484 | |||||||
| chr7:4714671 | C | T | 3 | a0001c0002t0002g0069 a0001c0003t0025g0254 a0001c0004t0035g0092 |
3 | HG02976.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.561-26167C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714671 | |||||||
| chr7:4714695 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.561-26143G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714695 | |||||||
| chr7:4714714 | T | TA | 5 | a0001c0001t0001g0017 a0001c0001t0001g0124 a0001c0001t0059g0231 others(2): Show |
5 | HG00621.hp1 HG00621.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-26123dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4714714 | ||||||
| chr7:4714725 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.561-26113G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714725 | |||||||
| chr7:4714822 | G | A | 2 | a0001c0001t0021g0012 a0001c0001t0021g0023 |
2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-26016G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714822 | |||||||
| chr7:4714879 | C | G | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-25959C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4714879 | |||||||
| chr7:4715098 | T | A | 2 | a0001c0001t0001g0205 a0001c0008t0003g0206 |
2 | NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.561-25740T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715098 | |||||||
| chr7:4715121 | T | C | 18 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(15): Show |
18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-25717T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715121 | |||||||
| chr7:4715136 | G | C | 2 | a0001c0003t0018g0207 a0001c0003t0018g0283 |
2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.561-25702G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715136 | |||||||
| chr7:4715143 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.561-25695T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715143 | |||||||
| chr7:4715151 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.561-25687C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715151 | |||||||
| chr7:4715171 | A | ACGATACG others(19): Show |
36 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(33): Show |
37 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-25641_561-2561 others(30): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4715171 | ||||||
| chr7:4715182 | C | CACGGTGG others(19): Show |
1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-25631_561-2563 others(30): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4715182 | ||||||
| chr7:4715226 | A | C | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-25612A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715226 | |||||||
| chr7:4715244 | T | C | 1 | a0001c0003t0096g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.561-25594T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715244 | |||||||
| chr7:4715252 | C | T | 2 | a0001c0001t0021g0012 a0001c0001t0021g0023 |
2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-25586C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715252 | |||||||
| chr7:4715281 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.561-25557A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715281 | |||||||
| chr7:4715333 | G | A | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-25505G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715333 | |||||||
| chr7:4715807 | T | A | 36 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(33): Show |
37 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-25031T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715807 | |||||||
| chr7:4715853 | C | A | 2 | a0001c0003t0062g0072 a0001c0003t0095g0073 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.561-24985C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715853 | |||||||
| chr7:4715863 | A | C | 36 | a0001c0001t0023g0015 a0001c0001t0047g0249 a0001c0002t0001g0047 others(33): Show |
37 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.561-24975A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715863 | |||||||
| chr7:4715924 | C | T | 18 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(15): Show |
18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-24914C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4715924 | |||||||
| chr7:4716018 | G | C | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-24820G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716018 | |||||||
| chr7:4716157 | G | A | 1 | a0001c0017t0016g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.561-24681G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716157 | |||||||
| chr7:4716202 | C | T | 7 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0025g0210 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-24636C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716202 | |||||||
| chr7:4716230 | C | CA | 6 | a0001c0001t0047g0249 a0001c0002t0001g0215 a0001c0002t0020g0285 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-24594dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4716230 | ||||||
| chr7:4716508 | A | C | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-24330A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716508 | |||||||
| chr7:4716646 | C | T | 11 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0001c0002t0063g0253 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-24192C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716646 | |||||||
| chr7:4716671 | C | T | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-24167C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716671 | |||||||
| chr7:4716674 | G | C | 6 | a0001c0002t0001g0257 a0001c0003t0017g0143 a0001c0003t0017g0173 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-24164G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716674 | |||||||
| chr7:4716792 | G | A | 18 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(15): Show |
18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-24046G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716792 | |||||||
| chr7:4716957 | G | A | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.561-23881G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4716957 | |||||||
| chr7:4717042 | G | A | 41 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(38): Show |
41 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.561-23796G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717042 | |||||||
| chr7:4717181 | G | C | 11 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-23657G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717181 | |||||||
| chr7:4717305 | A | G | 9 | a0001c0002t0001g0257 a0001c0003t0008g0262 a0001c0003t0017g0143 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-23533A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717305 | |||||||
| chr7:4717325 | G | A | 2 | a0001c0003t0018g0207 a0001c0003t0018g0283 |
2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.561-23513G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717325 | |||||||
| chr7:4717416 | A | G | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-23422A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717416 | |||||||
| chr7:4717440 | A | C | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-23398A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717440 | |||||||
| chr7:4717453 | GTGTGGCT others(8): Show |
G | 109 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(106): Show |
110 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(107): Show |
intron_variant | MODIFIER | c.561-23355_561-2334 others(19): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4717453 | ||||||
| chr7:4717473 | G | A | 11 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0001c0002t0063g0253 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-23365G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717473 | |||||||
| chr7:4717497 | C | T | 28 | a0001c0002t0002g0069 a0001c0002t0033g0103 a0001c0002t0046g0244 others(25): Show |
29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-23341C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717497 | |||||||
| chr7:4717503 | G | A | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-23335G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717503 | |||||||
| chr7:4717553 | C | G | 108 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(105): Show |
109 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.561-23285C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717553 | |||||||
| chr7:4717585 | C | T | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-23253C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717585 | |||||||
| chr7:4717760 | A | G | 38 | a0001c0001t0047g0249 a0001c0002t0001g0066 a0001c0002t0001g0257 others(35): Show |
38 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.561-23078A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717760 | |||||||
| chr7:4717792 | G | A | 7 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0025g0210 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-23046G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4717792 | |||||||
| chr7:4718213 | TGC | T | 28 | a0001c0002t0002g0069 a0001c0002t0033g0103 a0001c0002t0046g0244 others(25): Show |
29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-22622_561-2262 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4718213 | ||||||
| chr7:4718227 | T | C | 28 | a0001c0002t0002g0069 a0001c0002t0033g0103 a0001c0002t0046g0244 others(25): Show |
29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-22611T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718227 | |||||||
| chr7:4718243 | C | T | 11 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-22595C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718243 | |||||||
| chr7:4718255 | C | T | 10 | a0001c0003t0005g0247 a0001c0003t0011g0081 a0001c0003t0011g0236 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-22583C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718255 | |||||||
| chr7:4718268 | G | A | 1 | a0001c0004t0010g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.561-22570G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718268 | |||||||
| chr7:4718324 | A | C | 6 | a0001c0002t0001g0066 a0001c0002t0002g0282 a0001c0003t0015g0246 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-22514A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718324 | |||||||
| chr7:4718584 | C | A | 27 | a0001c0002t0002g0069 a0001c0002t0033g0103 a0001c0002t0046g0244 others(24): Show |
28 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.561-22254C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718584 | |||||||
| chr7:4718597 | C | T | 28 | a0001c0002t0002g0069 a0001c0002t0002g0227 a0001c0002t0002g0239 others(25): Show |
29 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561-22241C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718597 | |||||||
| chr7:4718598 | G | A | 8 | a0001c0003t0005g0247 a0001c0003t0011g0081 a0001c0003t0011g0236 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.561-22240G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718598 | |||||||
| chr7:4718626 | C | T | 2 | a0001c0003t0017g0143 a0001c0003t0092g0149 |
2 | HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.561-22212C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718626 | |||||||
| chr7:4718678 | G | A | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-22160G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718678 | |||||||
| chr7:4718750 | A | T | 19 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(16): Show |
19 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-22088A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718750 | |||||||
| chr7:4718852 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0062 |
2 | HG01361.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.561-21986C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718852 | |||||||
| chr7:4718925 | C | T | 101 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(98): Show |
102 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(99): Show |
intron_variant | MODIFIER | c.561-21913C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718925 | |||||||
| chr7:4718960 | C | T | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-21878C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718960 | |||||||
| chr7:4718982 | T | A | 3 | a0001c0002t0001g0127 a0001c0002t0001g0191 a0001c0002t0001g0215 |
3 | HG02056.hp2 HG02165.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.561-21856T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4718982 | |||||||
| chr7:4719029 | G | A | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-21809G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719029 | |||||||
| chr7:4719040 | C | T | 7 | a0001c0001t0001g0214 a0001c0004t0003g0120 a0001c0004t0007g0008 others(4): Show |
7 | NA18962.hp2 NA18995.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-21798C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719040 | |||||||
| chr7:4719089 | A | G | 3 | a0001c0003t0008g0262 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | HG02809.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-21749A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719089 | |||||||
| chr7:4719120 | GT | G | 16 | a0001c0002t0002g0282 a0001c0003t0005g0247 a0001c0003t0008g0262 others(13): Show |
16 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.561-21708delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4719120 | ||||||
| chr7:4719122 | T | G | 1 | a0001c0011t0004g0251 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.561-21716T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719122 | |||||||
| chr7:4719128 | TTTG | T | 55 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(52): Show |
56 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-21707_561-2170 others(7): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4719128 | ||||||
| chr7:4719130 | TG | T | 5 | a0001c0002t0074g0237 a0001c0003t0039g0082 a0001c0003t0062g0072 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-21707delG | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719130 | |||||||
| chr7:4719139 | T | G | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(74): Show |
78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21699T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719139 | |||||||
| chr7:4719140 | G | T | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(74): Show |
78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21698G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719140 | |||||||
| chr7:4719170 | C | G | 1 | a0001c0001t0049g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.561-21668C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719170 | |||||||
| chr7:4719179 | A | G | 84 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(81): Show |
85 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.561-21659A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719179 | |||||||
| chr7:4719189 | C | T | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-21649C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719189 | |||||||
| chr7:4719260 | G | A | 6 | a0001c0002t0001g0257 a0001c0003t0017g0143 a0001c0003t0017g0173 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-21578G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719260 | |||||||
| chr7:4719382 | C | T | 48 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(45): Show |
48 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.561-21456C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719382 | |||||||
| chr7:4719494 | A | T | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(74): Show |
78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21344A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719494 | |||||||
| chr7:4719543 | G | A | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-21295G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719543 | |||||||
| chr7:4719592 | C | G | 1 | a0006c0020t0037g0218 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.561-21246C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719592 | |||||||
| chr7:4719698 | T | TC | 47 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.561-21139dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4719698 | ||||||
| chr7:4719725 | A | G | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(74): Show |
78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-21113A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719725 | |||||||
| chr7:4719851 | T | C | 1 | a0001c0003t0018g0283 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.561-20987T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719851 | |||||||
| chr7:4719911 | G | A | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(74): Show |
78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-20927G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4719911 | |||||||
| chr7:4720088 | C | A | 14 | a0001c0002t0074g0237 a0001c0003t0005g0247 a0001c0003t0008g0262 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.561-20750C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720088 | |||||||
| chr7:4720266 | T | G | 1 | a0001c0003t0031g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.561-20572T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720266 | |||||||
| chr7:4720276 | G | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-20562G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720276 | |||||||
| chr7:4720322 | A | AC | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(74): Show |
78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-20515dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4720322 | ||||||
| chr7:4720381 | T | C | 1 | a0001c0023t0041g0105 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.561-20457T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720381 | |||||||
| chr7:4720420 | T | G | 1 | a0001c0017t0016g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.561-20418T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720420 | |||||||
| chr7:4720471 | T | G | 10 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-20367T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720471 | |||||||
| chr7:4720493 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
120 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.561-20345A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720493 | |||||||
| chr7:4720600 | G | A | 6 | a0001c0002t0001g0257 a0001c0003t0017g0143 a0001c0003t0017g0173 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-20238G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720600 | |||||||
| chr7:4720631 | C | G | 4 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0002c0012t0019g0290 others(1): Show |
4 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-20207C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720631 | |||||||
| chr7:4720638 | G | C | 7 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0025g0210 others(4): Show |
7 | HG01496.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-20200G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720638 | |||||||
| chr7:4720669 | T | C | 2 | a0001c0002t0002g0282 a0001c0003t0015g0246 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-20169T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720669 | |||||||
| chr7:4720692 | C | T | 10 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-20146C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720692 | |||||||
| chr7:4720708 | CT | C | 42 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(39): Show |
42 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.561-20117delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4720708 | ||||||
| chr7:4720763 | G | A | 10 | a0001c0002t0074g0237 a0001c0003t0005g0247 a0001c0003t0008g0262 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-20075G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720763 | |||||||
| chr7:4720768 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.561-20070C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720768 | |||||||
| chr7:4720828 | C | A | 2 | a0001c0002t0002g0282 a0001c0003t0015g0246 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-20010C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720828 | |||||||
| chr7:4720849 | C | G | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(74): Show |
78 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.561-19989C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720849 | |||||||
| chr7:4720922 | G | GA | 7 | a0001c0001t0020g0224 a0001c0002t0001g0257 a0001c0003t0017g0143 others(4): Show |
7 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-19906dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4720922 | ||||||
| chr7:4720970 | T | A | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-19868T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4720970 | |||||||
| chr7:4721018 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.561-19820C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721018 | |||||||
| chr7:4721052 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.561-19786A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721052 | |||||||
| chr7:4721065 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(159): Show |
163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.561-19773C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721065 | |||||||
| chr7:4721082 | G | A | 1 | a0001c0002t0063g0253 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.561-19756G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721082 | |||||||
| chr7:4721094 | C | G | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-19744C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721094 | |||||||
| chr7:4721114 | C | T | 18 | a0001c0002t0002g0227 a0001c0002t0002g0239 a0001c0002t0002g0240 others(15): Show |
18 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-19724C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721114 | |||||||
| chr7:4721161 | C | T | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-19677C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721161 | |||||||
| chr7:4721190 | G | T | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-19648G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721190 | |||||||
| chr7:4721237 | C | T | 6 | a0001c0002t0001g0257 a0001c0003t0017g0143 a0001c0003t0017g0173 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-19601C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721237 | |||||||
| chr7:4721313 | G | A | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-19525G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721313 | |||||||
| chr7:4721328 | C | T | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-19510C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721328 | |||||||
| chr7:4721329 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.561-19509G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721329 | |||||||
| chr7:4721367 | G | T | 1 | a0001c0004t0084g0109 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.561-19471G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721367 | |||||||
| chr7:4721389 | G | A | 25 | a0001c0001t0047g0249 a0001c0002t0001g0257 a0001c0002t0002g0227 others(22): Show |
25 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.561-19449G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721389 | |||||||
| chr7:4721572 | T | C | 1 | a0001c0007t0078g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.561-19266T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721572 | |||||||
| chr7:4721580 | C | T | 1 | a0001c0001t0006g0041 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.561-19258C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721580 | |||||||
| chr7:4721581 | TTTTTTTT others(1): Show |
T | 26 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(23): Show |
26 | HG01496.hp2 HG01891.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.561-19249_561-1924 others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721581 | ||||||
| chr7:4721589 | C | CT | 49 | a0001c0001t0001g0013 a0001c0001t0001g0138 a0001c0001t0001g0162 others(46): Show |
50 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.561-19230dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721589 | ||||||
| chr7:4721589 | C | T | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.561-19249C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721589 | |||||||
| chr7:4721589 | CT | C | 30 | a0001c0001t0001g0063 a0001c0001t0001g0192 a0001c0001t0023g0015 others(27): Show |
30 | HG00544.hp1 HG01123.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.561-19230delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721589 | ||||||
| chr7:4721589 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0190 a0001c0005t0014g0169 |
3 | HG00673.hp1 HG01981.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.561-19240_561-1923 others(15): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721589 | ||||||
| chr7:4721604 | T | G | 1 | a0001c0001t0057g0019 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.561-19234T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721604 | |||||||
| chr7:4721621 | T | G | 1 | a0001c0003t0026g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.561-19217T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721621 | |||||||
| chr7:4721659 | T | C | 3 | a0001c0001t0021g0012 a0001c0001t0021g0023 a0001c0004t0028g0028 |
3 | HG01175.hp2 HG01515.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.561-19179T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721659 | |||||||
| chr7:4721725 | GGATTACA others(128): Show |
G | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.561-19097_561-1896 others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4721725 | ||||||
| chr7:4721825 | A | T | 1 | a0001c0001t0052g0146 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.561-19013A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721825 | |||||||
| chr7:4721843 | G | C | 2 | a0001c0001t0001g0172 a0001c0024t0001g0212 |
2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.561-18995G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721843 | |||||||
| chr7:4721871 | G | T | 1 | a0001c0002t0001g0161 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.561-18967G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721871 | |||||||
| chr7:4721982 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.561-18856C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721982 | |||||||
| chr7:4721985 | A | C | 7 | a0001c0002t0020g0285 a0001c0003t0002g0238 a0001c0003t0012g0229 others(4): Show |
7 | HG01496.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-18853A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721985 | |||||||
| chr7:4721991 | G | C | 7 | a0001c0001t0001g0214 a0001c0004t0003g0120 a0001c0004t0007g0008 others(4): Show |
7 | NA18962.hp2 NA18995.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-18847G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4721991 | |||||||
| chr7:4722007 | A | T | 2 | a0001c0001t0067g0094 a0001c0003t0062g0072 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.561-18831A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722007 | |||||||
| chr7:4722076 | A | G | 35 | a0001c0001t0067g0094 a0001c0002t0002g0069 a0001c0002t0002g0240 others(32): Show |
36 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.561-18762A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722076 | |||||||
| chr7:4722215 | G | A | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-18623G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722215 | |||||||
| chr7:4722215 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.561-18623G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722215 | |||||||
| chr7:4722266 | TTCCCGAG others(2): Show |
T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(6): Show |
9 | HG00140.hp2 HG01106.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-18567_561-1855 others(13): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4722266 | ||||||
| chr7:4722512 | A | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(246): Show |
251 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.561-18326A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722512 | |||||||
| chr7:4722541 | G | A | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-18297G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722541 | |||||||
| chr7:4722564 | G | A | 2 | a0001c0003t0025g0210 a0001c0003t0082g0275 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.561-18274G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722564 | |||||||
| chr7:4722606 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.561-18232G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722606 | |||||||
| chr7:4722621 | A | T | 3 | a0001c0002t0001g0127 a0001c0002t0001g0191 a0001c0002t0001g0215 |
3 | HG02056.hp2 HG02165.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.561-18217A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722621 | |||||||
| chr7:4722699 | C | T | 19 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(16): Show |
19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-18139C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722699 | |||||||
| chr7:4722771 | C | T | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-18067C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722771 | |||||||
| chr7:4722789 | C | T | 37 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0125 others(34): Show |
37 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.561-18049C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722789 | |||||||
| chr7:4722914 | G | C | 3 | a0001c0003t0094g0286 a0001c0004t0097g0248 a0001c0011t0004g0280 |
3 | HG01496.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.561-17924G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722914 | |||||||
| chr7:4722921 | G | A | 2 | a0001c0001t0021g0012 a0001c0001t0021g0023 |
2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-17917G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4722921 | |||||||
| chr7:4723018 | G | A | 4 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0026g0079 others(1): Show |
4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-17820G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723018 | |||||||
| chr7:4723025 | T | C | 5 | a0001c0006t0013g0075 a0001c0006t0013g0076 a0001c0006t0013g0077 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-17813T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723025 | |||||||
| chr7:4723027 | A | G | 2 | a0001c0003t0062g0072 a0001c0003t0095g0073 |
2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.561-17811A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723027 | |||||||
| chr7:4723223 | G | A | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-17615G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723223 | |||||||
| chr7:4723390 | G | T | 3 | a0001c0003t0094g0286 a0001c0004t0097g0248 a0001c0011t0004g0280 |
3 | HG01496.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.561-17448G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723390 | |||||||
| chr7:4723526 | A | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(253): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.561-17312A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723526 | |||||||
| chr7:4723541 | C | T | 1 | a0001c0004t0084g0109 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.561-17297C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723541 | |||||||
| chr7:4723568 | C | A | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-17270C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723568 | |||||||
| chr7:4723584 | G | A | 1 | a0001c0007t0078g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.561-17254G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723584 | |||||||
| chr7:4723594 | C | T | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-17244C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723594 | |||||||
| chr7:4723599 | C | T | 2 | a0001c0001t0021g0012 a0001c0001t0021g0023 |
2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-17239C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723599 | |||||||
| chr7:4723611 | G | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-17227G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723611 | |||||||
| chr7:4723863 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(249): Show |
254 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.561-16975A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723863 | |||||||
| chr7:4723884 | C | T | 1 | a0001c0003t0092g0149 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.561-16954C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723884 | |||||||
| chr7:4723911 | T | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-16927T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4723911 | |||||||
| chr7:4723988 | CT | C | 24 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0002g0282 others(21): Show |
25 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.561-16848delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4723988 | ||||||
| chr7:4724079 | C | G | 5 | a0001c0002t0066g0209 a0001c0003t0080g0060 a0001c0003t0094g0286 others(2): Show |
5 | HG01496.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-16759C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724079 | |||||||
| chr7:4724114 | C | T | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-16724C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724114 | |||||||
| chr7:4724190 | G | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(193): Show |
198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.561-16648G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724190 | |||||||
| chr7:4724194 | G | A | 9 | a0001c0001t0019g0241 a0001c0001t0047g0249 a0001c0003t0096g0004 others(6): Show |
9 | HG02615.hp2 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-16644G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724194 | |||||||
| chr7:4724230 | C | T | 2 | a0001c0001t0021g0012 a0001c0001t0021g0023 |
2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-16608C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724230 | |||||||
| chr7:4724283 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(249): Show |
254 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.561-16555T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724283 | |||||||
| chr7:4724320 | C | G | 1 | a0001c0002t0020g0285 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.561-16518C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724320 | |||||||
| chr7:4724329 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(179): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.561-16509G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724329 | |||||||
| chr7:4724421 | C | G | 2 | a0001c0003t0017g0143 a0001c0003t0092g0149 |
2 | HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.561-16417C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724421 | |||||||
| chr7:4724428 | T | C | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-16410T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724428 | |||||||
| chr7:4724475 | C | T | 1 | a0001c0002t0002g0282 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.561-16363C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724475 | |||||||
| chr7:4724580 | A | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-16258A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724580 | |||||||
| chr7:4724582 | CAG | C | 3 | a0001c0002t0001g0066 a0001c0004t0038g0010 a0001c0007t0004g0234 |
3 | HG02630.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.561-16255_561-1625 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724582 | |||||||
| chr7:4724612 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
56 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.561-16226C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724612 | |||||||
| chr7:4724613 | G | A | 3 | a0001c0001t0001g0190 a0001c0002t0020g0285 a0001c0003t0012g0229 |
3 | HG02015.hp2 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-16225G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724613 | |||||||
| chr7:4724627 | C | T | 3 | a0001c0001t0001g0187 a0001c0003t0086g0213 a0001c0005t0014g0169 |
3 | HG00673.hp1 HG01981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.561-16211C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724627 | |||||||
| chr7:4724628 | G | A | 18 | a0001c0002t0002g0282 a0001c0002t0033g0103 a0001c0002t0046g0244 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.561-16210G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724628 | |||||||
| chr7:4724663 | C | G | 1 | a0001c0002t0001g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.561-16175C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724663 | |||||||
| chr7:4724691 | C | A | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-16147C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724691 | |||||||
| chr7:4724810 | G | C | 1 | a0001c0004t0011g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.561-16028G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724810 | |||||||
| chr7:4724831 | T | C | 2 | a0001c0003t0002g0238 a0001c0003t0015g0246 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.561-16007T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724831 | |||||||
| chr7:4724835 | T | C | 1 | a0001c0002t0001g0195 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.561-16003T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724835 | |||||||
| chr7:4724859 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.561-15979C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4724859 | |||||||
| chr7:4725079 | C | G | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-15759C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725079 | |||||||
| chr7:4725136 | T | G | 255 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(252): Show |
256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.561-15702T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725136 | |||||||
| chr7:4725137 | C | T | 2 | a0001c0015t0009g0225 a0001c0015t0009g0279 |
2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.561-15701C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725137 | |||||||
| chr7:4725140 | G | A | 4 | a0001c0002t0020g0285 a0001c0002t0066g0209 a0001c0003t0012g0229 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-15698G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725140 | |||||||
| chr7:4725191 | G | A | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-15647G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725191 | |||||||
| chr7:4725230 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.561-15608G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725230 | |||||||
| chr7:4725257 | G | A | 58 | a0001c0002t0001g0066 a0001c0002t0002g0068 a0001c0002t0002g0125 others(55): Show |
58 | HG01081.hp2 HG01109.hp1 HG01496.hp1 others(55): Show |
intron_variant | MODIFIER | c.561-15581G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725257 | |||||||
| chr7:4725264 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.561-15574G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725264 | |||||||
| chr7:4725272 | C | G | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-15566C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725272 | |||||||
| chr7:4725292 | C | T | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-15546C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725292 | |||||||
| chr7:4725347 | G | T | 2 | a0001c0003t0031g0005 a0001c0003t0039g0082 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.561-15491G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725347 | |||||||
| chr7:4725387 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(158): Show |
162 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.561-15451A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725387 | |||||||
| chr7:4725387 | A | T | 1 | a0001c0003t0086g0213 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.561-15451A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725387 | |||||||
| chr7:4725460 | G | T | 2 | a0001c0003t0012g0067 a0001c0003t0012g0100 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.561-15378G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725460 | |||||||
| chr7:4725616 | C | T | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-15222C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725616 | |||||||
| chr7:4725621 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0004t0007g0144 |
3 | NA18969.hp1 NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.561-15217G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725621 | |||||||
| chr7:4725700 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.561-15138C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725700 | |||||||
| chr7:4725794 | G | T | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-15044G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725794 | |||||||
| chr7:4725858 | G | A | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-14980G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725858 | |||||||
| chr7:4725916 | A | T | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-14922A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725916 | |||||||
| chr7:4725938 | G | A | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-14900G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4725938 | |||||||
| chr7:4726009 | A | G | 5 | a0001c0002t0002g0282 a0001c0003t0062g0072 a0001c0003t0096g0004 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-14829A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726009 | |||||||
| chr7:4726015 | C | CT | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(165): Show |
169 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.561-14810dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4726015 | ||||||
| chr7:4726015 | C | T | 2 | a0001c0003t0024g0071 a0001c0003t0024g0088 |
2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.561-14823C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726015 | |||||||
| chr7:4726015 | CT | C | 6 | a0001c0003t0005g0247 a0001c0003t0008g0262 a0001c0003t0011g0081 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-14810delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4726015 | ||||||
| chr7:4726115 | G | A | 2 | a0001c0004t0028g0028 a0001c0004t0029g0029 |
2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.561-14723G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726115 | |||||||
| chr7:4726146 | A | G | 19 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(16): Show |
19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-14692A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726146 | |||||||
| chr7:4726180 | T | C | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-14658T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726180 | |||||||
| chr7:4726293 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.561-14545C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726293 | |||||||
| chr7:4726479 | G | A | 1 | a0001c0027t0001g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.561-14359G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726479 | |||||||
| chr7:4726621 | C | CA | 24 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0057g0019 others(21): Show |
24 | HG00544.hp2 HG00738.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.561-14204dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4726621 | ||||||
| chr7:4726752 | A | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(233): Show |
238 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.561-14086A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726752 | |||||||
| chr7:4726764 | G | A | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-14074G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726764 | |||||||
| chr7:4726771 | C | A | 1 | a0001c0001t0006g0041 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.561-14067C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4726771 | |||||||
| chr7:4727019 | A | C | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-13819A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727019 | |||||||
| chr7:4727045 | A | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(156): Show |
160 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.561-13793A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727045 | |||||||
| chr7:4727207 | C | G | 1 | a0001c0002t0002g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.561-13631C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727207 | |||||||
| chr7:4727231 | C | T | 1 | a0001c0004t0010g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.561-13607C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727231 | |||||||
| chr7:4727292 | T | C | 10 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0001c0002t0063g0253 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.561-13546T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727292 | |||||||
| chr7:4727412 | T | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(199): Show |
203 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.561-13426T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727412 | |||||||
| chr7:4727481 | A | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(198): Show |
202 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.561-13357A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727481 | |||||||
| chr7:4727511 | C | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-13327C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727511 | |||||||
| chr7:4727514 | C | T | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-13324C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727514 | |||||||
| chr7:4727609 | C | T | 10 | a0001c0003t0005g0247 a0001c0003t0008g0262 a0001c0003t0011g0081 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-13229C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727609 | |||||||
| chr7:4727610 | G | A | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-13228G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727610 | |||||||
| chr7:4727653 | T | C | 1 | a0001c0004t0010g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.561-13185T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727653 | |||||||
| chr7:4727658 | C | T | 5 | a0001c0002t0020g0285 a0001c0002t0066g0209 a0001c0003t0012g0229 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-13180C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727658 | |||||||
| chr7:4727663 | G | C | 1 | a0001c0003t0080g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.561-13175G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727663 | |||||||
| chr7:4727700 | C | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-13138C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727700 | |||||||
| chr7:4727869 | G | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-12969G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4727869 | |||||||
| chr7:4728115 | C | T | 1 | a0001c0001t0067g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561-12723C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728115 | |||||||
| chr7:4728302 | C | T | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-12536C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728302 | |||||||
| chr7:4728359 | G | C | 1 | a0001c0001t0047g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.561-12479G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728359 | |||||||
| chr7:4728374 | C | T | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-12464C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728374 | |||||||
| chr7:4728379 | C | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-12459C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728379 | |||||||
| chr7:4728407 | T | C | 22 | a0001c0001t0023g0015 a0001c0002t0001g0047 a0001c0002t0001g0107 others(19): Show |
23 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.561-12431T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728407 | |||||||
| chr7:4728426 | C | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-12412C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728426 | |||||||
| chr7:4728458 | C | A | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-12380C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728458 | |||||||
| chr7:4728632 | T | A | 1 | a0001c0002t0060g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.561-12206T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728632 | |||||||
| chr7:4728683 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.561-12155G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728683 | |||||||
| chr7:4728730 | G | GA | 206 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(203): Show |
208 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.561-12087dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4728730 | ||||||
| chr7:4728730 | G | GAA | 7 | a0001c0001t0001g0162 a0001c0001t0022g0220 a0001c0001t0054g0129 others(4): Show |
7 | HG01106.hp1 HG01258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-12088_561-1208 others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4728730 | ||||||
| chr7:4728746 | A | G | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-12092A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728746 | |||||||
| chr7:4728748 | A | AG | 7 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0074g0237 others(4): Show |
7 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-12090_561-1208 others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728748 | |||||||
| chr7:4728772 | T | C | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-12066T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728772 | |||||||
| chr7:4728835 | G | A | 15 | a0001c0001t0023g0015 a0001c0002t0001g0047 a0001c0002t0001g0107 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.561-12003G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728835 | |||||||
| chr7:4728850 | G | T | 1 | a0001c0001t0043g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.561-11988G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4728850 | |||||||
| chr7:4729010 | C | T | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-11828C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729010 | |||||||
| chr7:4729034 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.561-11804A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729034 | |||||||
| chr7:4729183 | G | A | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-11655G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729183 | |||||||
| chr7:4729198 | G | A | 2 | a0001c0002t0002g0282 a0001c0003t0062g0072 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-11640G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729198 | |||||||
| chr7:4729208 | C | T | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-11630C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729208 | |||||||
| chr7:4729359 | C | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-11479C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729359 | |||||||
| chr7:4729373 | G | A | 2 | a0001c0002t0002g0282 a0001c0003t0062g0072 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561-11465G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729373 | |||||||
| chr7:4729398 | T | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(241): Show |
246 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.561-11440T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729398 | |||||||
| chr7:4729399 | T | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(237): Show |
242 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.561-11439T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729399 | |||||||
| chr7:4729536 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(157): Show |
161 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.561-11302C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729536 | |||||||
| chr7:4729663 | C | G | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-11175C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729663 | |||||||
| chr7:4729712 | G | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-11126G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729712 | |||||||
| chr7:4729772 | C | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-11066C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729772 | |||||||
| chr7:4729835 | C | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-11003C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729835 | |||||||
| chr7:4729981 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0057g0019 |
2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.561-10857C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4729981 | |||||||
| chr7:4730150 | A | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-10688A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730150 | |||||||
| chr7:4730208 | T | C | 2 | a0001c0002t0001g0132 a0001c0002t0001g0133 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.561-10630T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730208 | |||||||
| chr7:4730276 | C | T | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-10562C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730276 | |||||||
| chr7:4730443 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.561-10395C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730443 | |||||||
| chr7:4730508 | G | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-10330G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730508 | |||||||
| chr7:4730537 | G | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-10301G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730537 | |||||||
| chr7:4730567 | C | G | 2 | a0001c0002t0001g0222 a0001c0002t0001g0276 |
2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.561-10271C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730567 | |||||||
| chr7:4730627 | G | A | 1 | a0001c0007t0078g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.561-10211G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730627 | |||||||
| chr7:4730644 | G | A | 4 | a0001c0003t0002g0238 a0001c0003t0015g0246 a0001c0003t0026g0079 others(1): Show |
4 | HG02622.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-10194G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730644 | |||||||
| chr7:4730723 | C | T | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-10115C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730723 | |||||||
| chr7:4730900 | C | T | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-9938C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730900 | |||||||
| chr7:4730917 | A | G | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-9921A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730917 | |||||||
| chr7:4730932 | C | T | 19 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(16): Show |
19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-9906C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730932 | |||||||
| chr7:4730947 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0022g0003 a0001c0001t0022g0220 |
3 | NA18980.hp1 NA19060.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.561-9891C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4730947 | |||||||
| chr7:4731073 | C | T | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-9765C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731073 | |||||||
| chr7:4731124 | C | T | 1 | a0001c0004t0007g0233 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.561-9714C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731124 | |||||||
| chr7:4731140 | T | C | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-9698T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731140 | |||||||
| chr7:4731263 | C | T | 7 | a0001c0002t0020g0285 a0001c0003t0012g0067 a0001c0003t0012g0100 others(4): Show |
7 | HG02257.hp1 HG02647.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-9575C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731263 | |||||||
| chr7:4731315 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0110 |
2 | HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.561-9523G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731315 | |||||||
| chr7:4731384 | A | G | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-9454A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731384 | |||||||
| chr7:4731414 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.561-9424G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731414 | |||||||
| chr7:4731589 | A | G | 23 | a0001c0001t0047g0249 a0001c0002t0001g0098 a0001c0002t0001g0257 others(20): Show |
23 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.561-9249A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731589 | |||||||
| chr7:4731647 | C | G | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-9191C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731647 | |||||||
| chr7:4731746 | G | A | 1 | a0001c0001t0056g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.561-9092G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731746 | |||||||
| chr7:4731758 | C | CA | 21 | a0001c0001t0001g0201 a0001c0001t0022g0220 a0001c0001t0049g0039 others(18): Show |
21 | HG00735.hp2 HG02055.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.561-9061dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4731758 | ||||||
| chr7:4731758 | CAA | C | 13 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0066g0209 others(10): Show |
13 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.561-9062_561-9061d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4731758 | ||||||
| chr7:4731780 | A | G | 10 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0115 others(7): Show |
10 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-9058A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731780 | |||||||
| chr7:4731791 | C | T | 3 | a0001c0002t0066g0209 a0001c0003t0080g0060 a0001c0003t0091g0278 |
3 | HG02818.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.561-9047C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731791 | |||||||
| chr7:4731814 | C | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-9024C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731814 | |||||||
| chr7:4731904 | C | T | 6 | a0001c0002t0020g0285 a0001c0002t0074g0237 a0001c0003t0012g0229 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-8934C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731904 | |||||||
| chr7:4731950 | C | T | 1 | a0001c0007t0004g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561-8888C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731950 | |||||||
| chr7:4731958 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.561-8880G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4731958 | |||||||
| chr7:4732006 | C | T | 5 | a0001c0002t0020g0285 a0001c0002t0074g0237 a0001c0003t0012g0229 others(2): Show |
5 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-8832C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732006 | |||||||
| chr7:4732015 | T | C | 12 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0020g0285 others(9): Show |
12 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-8823T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732015 | |||||||
| chr7:4732071 | G | A | 1 | a0001c0003t0024g0088 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.561-8767G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732071 | |||||||
| chr7:4732154 | C | T | 1 | a0001c0004t0093g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.561-8684C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732154 | |||||||
| chr7:4732188 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG00544.hp2 NA18944.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-8650G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732188 | |||||||
| chr7:4732212 | T | C | 4 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0026g0079 others(1): Show |
4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-8626T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732212 | |||||||
| chr7:4732233 | C | G | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8605C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732233 | |||||||
| chr7:4732234 | T | C | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8604T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732234 | |||||||
| chr7:4732235 | G | A | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8603G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732235 | |||||||
| chr7:4732236 | A | C | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8602A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732236 | |||||||
| chr7:4732238 | T | C | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8600T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732238 | |||||||
| chr7:4732239 | A | C | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8599A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732239 | |||||||
| chr7:4732240 | T | A | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-8598T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732240 | |||||||
| chr7:4732244 | C | T | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-8594C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732244 | |||||||
| chr7:4732256 | C | T | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-8582C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732256 | |||||||
| chr7:4732330 | A | G | 2 | a0001c0001t0021g0012 a0001c0001t0021g0023 |
2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.561-8508A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732330 | |||||||
| chr7:4732347 | T | G | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-8491T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732347 | |||||||
| chr7:4732378 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.561-8460C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732378 | |||||||
| chr7:4732379 | G | A | 1 | a0001c0001t0065g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.561-8459G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732379 | |||||||
| chr7:4732386 | A | G | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-8452A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732386 | |||||||
| chr7:4732441 | C | T | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-8397C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732441 | |||||||
| chr7:4732524 | G | T | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-8314G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732524 | |||||||
| chr7:4732594 | G | A | 1 | a0001c0001t0030g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.561-8244G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732594 | |||||||
| chr7:4732606 | C | T | 1 | a0001c0001t0052g0146 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.561-8232C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732606 | |||||||
| chr7:4732872 | C | T | 7 | a0001c0002t0066g0209 a0001c0003t0012g0067 a0001c0003t0012g0100 others(4): Show |
7 | HG02257.hp1 HG02818.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-7966C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732872 | |||||||
| chr7:4732900 | C | T | 1 | a0001c0002t0044g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.561-7938C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732900 | |||||||
| chr7:4732917 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.561-7921G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4732917 | |||||||
| chr7:4733071 | G | C | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7767G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733071 | |||||||
| chr7:4733085 | C | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7753C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733085 | |||||||
| chr7:4733096 | C | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7742C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733096 | |||||||
| chr7:4733179 | C | CT | 6 | a0001c0002t0002g0282 a0001c0003t0062g0072 a0001c0003t0086g0213 others(3): Show |
6 | HG02622.hp2 NA18906.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-7648dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4733179 | ||||||
| chr7:4733190 | T | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-7648T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733190 | |||||||
| chr7:4733368 | C | G | 2 | a0001c0003t0094g0286 a0001c0011t0004g0280 |
2 | HG01496.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.561-7470C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733368 | |||||||
| chr7:4733386 | G | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0061 others(6): Show |
9 | HG00140.hp2 HG01106.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-7452G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733386 | |||||||
| chr7:4733520 | C | G | 7 | a0001c0001t0001g0214 a0001c0004t0003g0120 a0001c0004t0007g0008 others(4): Show |
7 | NA18962.hp2 NA18995.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-7318C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733520 | |||||||
| chr7:4733722 | C | G | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7116C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733722 | |||||||
| chr7:4733723 | G | T | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-7115G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733723 | |||||||
| chr7:4733775 | C | G | 1 | a0001c0002t0063g0253 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.561-7063C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733775 | |||||||
| chr7:4733947 | C | T | 1 | a0001c0003t0012g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.561-6891C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733947 | |||||||
| chr7:4733971 | G | GCTGGCCA others(16): Show |
13 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(10): Show |
13 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.561-6865_561-6843d others(25): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4733971 | ||||||
| chr7:4733979 | C | T | 2 | a0001c0001t0001g0259 a0001c0022t0001g0211 |
2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.561-6859C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4733979 | |||||||
| chr7:4734040 | G | C | 1 | a0001c0001t0023g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.561-6798G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734040 | |||||||
| chr7:4734139 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.561-6699C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734139 | |||||||
| chr7:4734390 | G | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0205 a0001c0001t0001g0221 |
3 | HG02129.hp2 NA18942.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.561-6448G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734390 | |||||||
| chr7:4734469 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.561-6369T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734469 | |||||||
| chr7:4734603 | G | A | 32 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0125 others(29): Show |
32 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.561-6235G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734603 | |||||||
| chr7:4734619 | G | C | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-6219G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734619 | |||||||
| chr7:4734624 | C | T | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-6214C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734624 | |||||||
| chr7:4734625 | A | G | 1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-6213A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734625 | |||||||
| chr7:4734765 | C | T | 1 | a0003c0014t0001g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.561-6073C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734765 | |||||||
| chr7:4734854 | G | A | 4 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0026g0079 others(1): Show |
4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-5984G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734854 | |||||||
| chr7:4734972 | A | T | 21 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0020g0285 others(18): Show |
21 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.561-5866A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4734972 | |||||||
| chr7:4735373 | C | T | 6 | a0001c0002t0020g0285 a0001c0002t0074g0237 a0001c0003t0012g0229 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-5465C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735373 | |||||||
| chr7:4735418 | G | A | 2 | a0001c0003t0012g0067 a0001c0003t0012g0100 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.561-5420G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735418 | |||||||
| chr7:4735511 | C | G | 1 | a0001c0004t0035g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.561-5327C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735511 | |||||||
| chr7:4735544 | C | T | 2 | a0001c0003t0025g0210 a0001c0003t0082g0275 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.561-5294C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735544 | |||||||
| chr7:4735648 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.561-5190G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735648 | |||||||
| chr7:4735735 | C | T | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-5103C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735735 | |||||||
| chr7:4735736 | G | A | 1 | a0001c0004t0089g0198 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.561-5102G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735736 | |||||||
| chr7:4735750 | C | T | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-5088C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735750 | |||||||
| chr7:4735766 | C | T | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-5072C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735766 | |||||||
| chr7:4735835 | C | G | 1 | a0001c0007t0004g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561-5003C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735835 | |||||||
| chr7:4735839 | G | A | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-4999G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735839 | |||||||
| chr7:4735844 | T | C | 22 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0020g0285 others(19): Show |
22 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.561-4994T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735844 | |||||||
| chr7:4735860 | A | G | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-4978A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735860 | |||||||
| chr7:4735876 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(233): Show |
238 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.561-4962A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4735876 | |||||||
| chr7:4736414 | G | GT | 18 | a0001c0001t0001g0230 a0001c0001t0042g0139 a0001c0001t0049g0039 others(15): Show |
18 | HG01081.hp1 HG01175.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.561-4408dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4736414 | ||||||
| chr7:4736414 | G | T | 10 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-4424G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736414 | |||||||
| chr7:4736767 | A | G | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-4071A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736767 | |||||||
| chr7:4736849 | G | T | 19 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(16): Show |
19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-3989G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736849 | |||||||
| chr7:4736916 | A | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(229): Show |
234 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.561-3922A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4736916 | |||||||
| chr7:4737425 | GGTGTGTG others(7): Show |
G | 4 | a0001c0002t0066g0209 a0001c0003t0080g0060 a0001c0003t0091g0278 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-3402_561-3389d others(16): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737425 | ||||||
| chr7:4737439 | CGT | C | 65 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(62): Show |
65 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.561-3391_561-3390d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737439 | ||||||
| chr7:4737447 | T | C | 1 | a0001c0004t0003g0120 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.561-3391T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737447 | |||||||
| chr7:4737462 | ATG | A | 5 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-3365_561-3364d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737462 | ||||||
| chr7:4737471 | T | C | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.561-3367T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737471 | |||||||
| chr7:4737475 | C | T | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-3363C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737475 | |||||||
| chr7:4737484 | G | A | 1 | a0001c0010t0079g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.561-3354G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737484 | |||||||
| chr7:4737530 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(237): Show |
242 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.561-3308A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737530 | |||||||
| chr7:4737540 | G | A | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561-3298G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737540 | |||||||
| chr7:4737551 | C | CGTGTGTG others(3): Show |
2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-3287_561-3286i others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737551 | |||||||
| chr7:4737551 | C | CGTGTGTG others(17): Show |
2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-3287_561-3286i others(26): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737551 | |||||||
| chr7:4737552 | C | CTG | 15 | a0001c0001t0001g0102 a0001c0001t0065g0203 a0001c0002t0001g0127 others(12): Show |
15 | HG02055.hp2 HG02056.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.561-3265_561-3264d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | ||||||
| chr7:4737552 | C | CTGTG | 180 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(177): Show |
181 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.561-3267_561-3264d others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | ||||||
| chr7:4737552 | C | CTGTGTG | 12 | a0001c0001t0001g0192 a0001c0001t0001g0230 a0001c0001t0001g0265 others(9): Show |
13 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.561-3269_561-3264d others(8): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | ||||||
| chr7:4737552 | C | CTGTGTGT others(1): Show |
6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-3271_561-3264d others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | ||||||
| chr7:4737552 | C | CTGTGTGT others(3): Show |
2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-3273_561-3264d others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | ||||||
| chr7:4737552 | C | CTGTGTGT others(5): Show |
3 | a0001c0003t0094g0286 a0001c0003t0095g0073 a0001c0011t0004g0280 |
3 | HG01496.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.561-3275_561-3264d others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | ||||||
| chr7:4737552 | C | CTGTGTGT others(9): Show |
1 | a0001c0002t0074g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-3279_561-3264d others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737552 | ||||||
| chr7:4737552 | C | G | 4 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0026g0079 others(1): Show |
4 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-3286C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737552 | |||||||
| chr7:4737569 | T | TGTGTGTG others(3): Show |
10 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0115 others(7): Show |
10 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-3264_561-3263i others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737569 | ||||||
| chr7:4737573 | T | TGTGTGTG others(9): Show |
1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.561-3264_561-3263i others(18): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4737573 | ||||||
| chr7:4737581 | T | G | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.561-3257T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737581 | |||||||
| chr7:4737624 | G | A | 1 | a0001c0003t0099g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.561-3214G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737624 | |||||||
| chr7:4737808 | A | T | 21 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0020g0285 others(18): Show |
21 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.561-3030A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737808 | |||||||
| chr7:4737861 | G | A | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.561-2977G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737861 | |||||||
| chr7:4737999 | G | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561-2839G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4737999 | |||||||
| chr7:4738130 | GAA | G | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-2694_561-2693d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738130 | ||||||
| chr7:4738133 | A | G | 6 | a0001c0002t0020g0285 a0001c0002t0074g0237 a0001c0003t0012g0229 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-2705A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738133 | |||||||
| chr7:4738225 | T | C | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-2613T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738225 | |||||||
| chr7:4738246 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0054g0129 |
2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.561-2592G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738246 | |||||||
| chr7:4738265 | C | T | 10 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0115 others(7): Show |
10 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-2573C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738265 | |||||||
| chr7:4738295 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0020 others(39): Show |
43 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.561-2543G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738295 | |||||||
| chr7:4738322 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.561-2516A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738322 | |||||||
| chr7:4738393 | C | T | 1 | a0001c0004t0011g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.561-2445C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738393 | |||||||
| chr7:4738436 | CA | C | 16 | a0001c0001t0001g0119 a0001c0002t0001g0200 a0001c0002t0001g0215 others(13): Show |
16 | HG00408.hp2 HG01496.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.561-2388delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738436 | ||||||
| chr7:4738436 | CAA | C | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-2389_561-2388d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738436 | ||||||
| chr7:4738664 | C | T | 10 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0012g0067 others(7): Show |
10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-2174C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738664 | |||||||
| chr7:4738665 | G | A | 1 | a0001c0001t0065g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.561-2173G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4738665 | |||||||
| chr7:4738949 | G | GGGAAGAA others(3): Show |
3 | a0001c0003t0002g0238 a0001c0003t0015g0246 a0001c0003t0025g0254 |
3 | HG02622.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.561-1887_561-1878d others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4738949 | ||||||
| chr7:4739416 | T | C | 3 | a0001c0001t0047g0249 a0001c0002t0066g0209 a0001c0003t0080g0060 |
3 | HG02723.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.561-1422T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739416 | |||||||
| chr7:4739420 | TTTG | T | 7 | a0001c0002t0002g0282 a0001c0003t0062g0072 a0001c0006t0013g0075 others(4): Show |
7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-1415_561-1413d others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4739420 | ||||||
| chr7:4739484 | A | G | 3 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 |
3 | HG02717.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.561-1354A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739484 | |||||||
| chr7:4739652 | G | C | 1 | a0001c0010t0001g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.561-1186G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739652 | |||||||
| chr7:4739700 | T | A | 19 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(16): Show |
19 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.561-1138T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739700 | |||||||
| chr7:4739833 | C | T | 1 | a0001c0002t0002g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.561-1005C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739833 | |||||||
| chr7:4739980 | T | C | 18 | a0001c0002t0002g0282 a0001c0002t0020g0285 a0001c0002t0066g0209 others(15): Show |
18 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.561-858T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4739980 | |||||||
| chr7:4739987 | TCA | T | 9 | a0001c0003t0005g0247 a0001c0003t0008g0262 a0001c0003t0011g0081 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.561-844_561-843del others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4739987 | ||||||
| chr7:4740043 | C | G | 1 | a0001c0001t0052g0146 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.561-795C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740043 | |||||||
| chr7:4740059 | C | T | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.561-779C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740059 | |||||||
| chr7:4740168 | C | T | 1 | a0001c0003t0081g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.561-670C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740168 | |||||||
| chr7:4740169 | G | T | 12 | a0001c0002t0002g0282 a0001c0002t0066g0209 a0001c0003t0062g0072 others(9): Show |
12 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-669G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740169 | |||||||
| chr7:4740251 | A | G | 6 | a0001c0002t0020g0285 a0001c0002t0074g0237 a0001c0003t0012g0229 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-587A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740251 | |||||||
| chr7:4740262 | C | G | 1 | a0001c0003t0096g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.561-576C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740262 | |||||||
| chr7:4740274 | T | C | 28 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0002g0282 others(25): Show |
28 | HG01081.hp1 HG01081.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.561-564T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740274 | |||||||
| chr7:4740292 | T | C | 4 | a0001c0004t0005g0263 a0001c0007t0004g0084 a0001c0007t0004g0085 others(1): Show |
4 | HG02145.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-546T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740292 | |||||||
| chr7:4740322 | C | T | 5 | a0001c0002t0020g0285 a0001c0002t0074g0237 a0001c0003t0012g0229 others(2): Show |
5 | HG02647.hp1 NA18522.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-516C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740322 | |||||||
| chr7:4740371 | A | G | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-467A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740371 | |||||||
| chr7:4740388 | T | C | 1 | a0001c0003t0017g0173 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.561-450T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740388 | |||||||
| chr7:4740390 | C | A | 1 | a0001c0003t0017g0173 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.561-448C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740390 | |||||||
| chr7:4740408 | C | T | 10 | a0001c0002t0002g0282 a0001c0002t0066g0209 a0001c0003t0062g0072 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.561-430C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740408 | |||||||
| chr7:4740413 | G | A | 8 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(5): Show |
8 | HG02109.hp1 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-425G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740413 | |||||||
| chr7:4740438 | A | T | 17 | a0001c0002t0002g0282 a0001c0002t0066g0209 a0001c0003t0002g0238 others(14): Show |
17 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.561-400A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740438 | |||||||
| chr7:4740483 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.561-355C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740483 | |||||||
| chr7:4740484 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.561-354G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740484 | |||||||
| chr7:4740572 | T | A | 2 | a0001c0004t0003g0120 a0001c0004t0007g0233 |
2 | NA18962.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.561-266T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740572 | |||||||
| chr7:4740583 | C | T | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-255C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740583 | |||||||
| chr7:4740592 | C | CAG | 28 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0002t0002g0282 others(25): Show |
28 | HG01081.hp1 HG01081.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.561-245_561-244dup others(2): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4740592 | ||||||
| chr7:4740596 | G | A | 3 | a0001c0002t0001g0066 a0001c0004t0038g0010 a0001c0007t0004g0234 |
3 | HG02630.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.561-242G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740596 | |||||||
| chr7:4740643 | A | C | 1 | a0001c0011t0004g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561-195A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740643 | |||||||
| chr7:4740807 | C | T | 1 | a0001c0002t0001g0148 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.561-31C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | chr7 | 4740807 | |||||||
| chr7:4740819 | GCTC | G | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.561-10_561-8delCCT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 4740819 | ||||||
| chr7:4741036 | C | G | 1 | a0001c0002t0002g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.746+13C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741036 | |||||||
| chr7:4741100 | C | T | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.746+77C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741100 | |||||||
| chr7:4741301 | T | C | 1 | a0001c0002t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.746+278T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741301 | |||||||
| chr7:4741312 | G | A | 229 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(226): Show |
231 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.746+289G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741312 | |||||||
| chr7:4741323 | GT | G | 43 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0125 others(40): Show |
43 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.746+310delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4741323 | ||||||
| chr7:4741330 | T | G | 171 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(168): Show |
173 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.746+307T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741330 | |||||||
| chr7:4741389 | C | T | 6 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0017g0143 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.746+366C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741389 | |||||||
| chr7:4741485 | C | G | 3 | a0001c0002t0074g0237 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+462C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741485 | |||||||
| chr7:4741532 | T | C | 14 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0002t0020g0285 others(11): Show |
14 | HG01081.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.746+509T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741532 | |||||||
| chr7:4741561 | C | T | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+538C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741561 | |||||||
| chr7:4741580 | C | T | 2 | a0001c0002t0001g0222 a0001c0002t0001g0276 |
2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.746+557C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741580 | |||||||
| chr7:4741622 | C | T | 5 | a0001c0001t0019g0241 a0001c0004t0011g0255 a0002c0012t0019g0290 others(2): Show |
5 | HG01109.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+599C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741622 | |||||||
| chr7:4741734 | A | G | 1 | a0001c0003t0096g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.746+711A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741734 | |||||||
| chr7:4741846 | G | A | 1 | a0001c0003t0091g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.746+823G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741846 | |||||||
| chr7:4741928 | T | G | 1 | a0001c0002t0001g0160 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.746+905T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4741928 | |||||||
| chr7:4742003 | C | T | 4 | a0001c0003t0002g0238 a0001c0003t0015g0246 a0001c0003t0094g0286 others(1): Show |
4 | HG01496.hp2 HG02622.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+980C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742003 | |||||||
| chr7:4742010 | T | G | 3 | a0001c0002t0074g0237 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+987T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742010 | |||||||
| chr7:4742045 | C | T | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.746+1022C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742045 | |||||||
| chr7:4742056 | C | T | 1 | a0001c0004t0010g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.746+1033C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742056 | |||||||
| chr7:4742073 | C | T | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.746+1050C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742073 | |||||||
| chr7:4742074 | G | A | 2 | a0001c0002t0020g0285 a0001c0003t0012g0229 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.746+1051G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742074 | |||||||
| chr7:4742298 | G | A | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.746+1275G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742298 | |||||||
| chr7:4742340 | C | T | 2 | a0001c0003t0012g0067 a0001c0003t0012g0100 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.746+1317C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742340 | |||||||
| chr7:4742455 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.746+1432C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742455 | |||||||
| chr7:4742536 | C | T | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+1513C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742536 | |||||||
| chr7:4742600 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.746+1577A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742600 | |||||||
| chr7:4742659 | C | T | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.746+1636C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742659 | |||||||
| chr7:4742722 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.746+1699A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742722 | |||||||
| chr7:4742916 | G | A | 1 | a0001c0008t0003g0095 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.746+1893G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742916 | |||||||
| chr7:4742965 | A | C | 11 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0012g0067 others(8): Show |
11 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.746+1942A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742965 | |||||||
| chr7:4742984 | C | T | 10 | a0001c0002t0001g0098 a0001c0002t0001g0257 a0001c0003t0012g0067 others(7): Show |
10 | HG01081.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+1961C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4742984 | |||||||
| chr7:4743012 | C | T | 1 | a0001c0003t0080g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.746+1989C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743012 | |||||||
| chr7:4743292 | C | G | 1 | a0001c0003t0073g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.746+2269C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743292 | |||||||
| chr7:4743443 | G | A | 9 | a0001c0003t0005g0247 a0001c0003t0008g0262 a0001c0003t0011g0081 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.746+2420G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743443 | |||||||
| chr7:4743486 | G | T | 4 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0025g0210 others(1): Show |
4 | HG02257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+2463G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743486 | |||||||
| chr7:4743512 | T | G | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.746+2489T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743512 | |||||||
| chr7:4743575 | T | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(226): Show |
231 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.746+2552T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743575 | |||||||
| chr7:4743593 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(159): Show |
164 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.746+2570A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743593 | |||||||
| chr7:4743622 | T | G | 1 | a0002c0013t0015g0287 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.746+2599T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743622 | |||||||
| chr7:4743677 | A | G | 7 | a0001c0002t0002g0282 a0001c0003t0062g0072 a0001c0006t0013g0075 others(4): Show |
7 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.746+2654A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743677 | |||||||
| chr7:4743822 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0110 |
2 | HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.746+2799C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743822 | |||||||
| chr7:4743823 | G | A | 3 | a0001c0002t0074g0237 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+2800G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743823 | |||||||
| chr7:4743878 | G | GC | 4 | a0001c0001t0021g0012 a0001c0001t0021g0023 a0001c0027t0001g0217 others(1): Show |
4 | HG00323.hp2 HG00621.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+2856dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4743878 | ||||||
| chr7:4743879 | CT | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0128 others(12): Show |
15 | HG01070.hp1 HG01081.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.746+2871delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4743879 | ||||||
| chr7:4743880 | T | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(162): Show |
167 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.746+2857T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743880 | |||||||
| chr7:4743881 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0128 others(1): Show |
4 | HG01256.hp2 HG02965.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+2858T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743881 | |||||||
| chr7:4743915 | C | T | 1 | a0001c0021t0016g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.746+2892C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4743915 | |||||||
| chr7:4744038 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.746+3015G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744038 | |||||||
| chr7:4744079 | G | T | 1 | a0002c0013t0015g0287 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.746+3056G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744079 | |||||||
| chr7:4744092 | G | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(176): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.746+3069G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744092 | |||||||
| chr7:4744135 | A | G | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.746+3112A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744135 | |||||||
| chr7:4744177 | G | GTT | 13 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0002t0066g0209 others(10): Show |
13 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.746+3154_746+3155i others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744177 | |||||||
| chr7:4744196 | T | C | 1 | a0001c0001t0023g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.746+3173T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744196 | |||||||
| chr7:4744231 | T | C | 1 | a0001c0002t0046g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.746+3208T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744231 | |||||||
| chr7:4744307 | C | T | 9 | a0001c0003t0005g0247 a0001c0003t0008g0262 a0001c0003t0011g0081 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.746+3284C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744307 | |||||||
| chr7:4744408 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.746+3385G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744408 | |||||||
| chr7:4744600 | G | C | 1 | a0001c0003t0008g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.746+3577G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744600 | |||||||
| chr7:4744609 | G | A | 1 | a0001c0008t0087g0271 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.746+3586G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744609 | |||||||
| chr7:4744779 | C | A | 3 | a0001c0002t0074g0237 a0001c0003t0026g0079 a0001c0003t0026g0080 |
3 | NA18522.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.746+3756C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744779 | |||||||
| chr7:4744999 | C | T | 3 | a0001c0002t0020g0285 a0001c0003t0012g0229 a0001c0003t0091g0278 |
3 | HG02647.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.746+3976C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4744999 | |||||||
| chr7:4745021 | T | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(176): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.746+3998T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745021 | |||||||
| chr7:4745135 | G | A | 1 | a0001c0002t0001g0178 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.746+4112G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745135 | |||||||
| chr7:4745185 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(179): Show |
184 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.746+4162A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745185 | |||||||
| chr7:4745246 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0110 |
2 | HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.746+4223C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745246 | |||||||
| chr7:4745378 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(121): Show |
125 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.746+4355G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745378 | |||||||
| chr7:4745392 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(114): Show |
118 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.746+4369C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745392 | |||||||
| chr7:4745472 | T | TTG | 166 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(163): Show |
168 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.746+4465_746+4466d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4745472 | ||||||
| chr7:4745498 | T | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(178): Show |
183 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.746+4475T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745498 | |||||||
| chr7:4745600 | T | A | 4 | a0001c0002t0033g0103 a0001c0002t0046g0244 a0001c0003t0018g0207 others(1): Show |
4 | HG01496.hp1 HG02055.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+4577T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745600 | |||||||
| chr7:4745655 | G | T | 1 | a0001c0002t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.746+4632G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745655 | |||||||
| chr7:4745731 | C | G | 1 | a0001c0003t0095g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.746+4708C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745731 | |||||||
| chr7:4745756 | G | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(183): Show |
188 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.746+4733G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745756 | |||||||
| chr7:4745773 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.746+4750C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745773 | |||||||
| chr7:4745884 | C | CA | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(179): Show |
184 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.746+4871dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4745884 | ||||||
| chr7:4745899 | T | C | 10 | a0001c0001t0047g0249 a0001c0002t0002g0282 a0001c0002t0066g0209 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.746+4876T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4745899 | |||||||
| chr7:4746129 | C | T | 2 | a0001c0003t0012g0067 a0001c0003t0012g0100 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.746+5106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746129 | |||||||
| chr7:4746146 | C | T | 1 | a0001c0003t0062g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.746+5123C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746146 | |||||||
| chr7:4746152 | A | G | 1 | a0001c0003t0025g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.746+5129A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746152 | |||||||
| chr7:4746249 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.746+5226C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746249 | |||||||
| chr7:4746430 | C | T | 2 | a0001c0002t0066g0209 a0001c0003t0080g0060 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.746+5407C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746430 | |||||||
| chr7:4746439 | G | A | 1 | a0001c0005t0001g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.746+5416G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746439 | |||||||
| chr7:4746494 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(247): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.746+5471G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746494 | |||||||
| chr7:4746503 | G | C | 5 | a0001c0001t0047g0249 a0001c0002t0033g0103 a0001c0002t0046g0244 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+5480G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746503 | |||||||
| chr7:4746537 | A | C | 1 | a0001c0003t0008g0262 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.746+5514A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4746537 | |||||||
| chr7:4747078 | G | A | 4 | a0001c0002t0001g0131 a0001c0002t0001g0160 a0001c0017t0016g0106 others(1): Show |
4 | HG00140.hp1 HG00639.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+6055G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747078 | |||||||
| chr7:4747132 | G | A | 1 | a0001c0001t0068g0052 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.746+6109G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747132 | |||||||
| chr7:4747170 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.746+6147G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747170 | |||||||
| chr7:4747241 | C | T | 10 | a0001c0001t0001g0204 a0001c0001t0023g0015 a0001c0001t0054g0129 others(7): Show |
10 | HG01074.hp1 HG01109.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+6218C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747241 | |||||||
| chr7:4747252 | C | T | 7 | a0001c0001t0067g0094 a0001c0002t0002g0282 a0001c0003t0018g0283 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.746+6229C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747252 | |||||||
| chr7:4747253 | G | A | 2 | a0001c0002t0033g0103 a0001c0003t0091g0278 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.746+6230G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747253 | |||||||
| chr7:4747268 | C | T | 1 | a0001c0001t0006g0258 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.746+6245C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747268 | |||||||
| chr7:4747333 | C | T | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.746+6310C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747333 | |||||||
| chr7:4747356 | G | A | 1 | a0001c0007t0004g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.746+6333G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747356 | |||||||
| chr7:4747368 | A | G | 25 | a0001c0002t0002g0069 a0001c0002t0002g0125 a0001c0002t0002g0126 others(22): Show |
25 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.746+6345A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747368 | |||||||
| chr7:4747378 | G | A | 16 | a0001c0001t0047g0249 a0001c0001t0067g0094 a0001c0002t0002g0069 others(13): Show |
16 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+6355G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747378 | |||||||
| chr7:4747387 | A | G | 1 | a0001c0002t0063g0253 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.746+6364A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747387 | |||||||
| chr7:4747461 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(101): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.746+6438A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747461 | |||||||
| chr7:4747629 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.746+6606G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747629 | |||||||
| chr7:4747729 | T | G | 1 | a0001c0002t0001g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.746+6706T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747729 | |||||||
| chr7:4747752 | A | G | 3 | a0001c0009t0003g0142 a0001c0009t0003g0164 a0001c0009t0003g0165 |
3 | NA18969.hp2 NA19066.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.747-6707A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747752 | |||||||
| chr7:4747779 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.747-6680C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747779 | |||||||
| chr7:4747799 | A | C | 14 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(11): Show |
14 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.747-6660A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747799 | |||||||
| chr7:4747877 | G | A | 5 | a0001c0003t0017g0143 a0001c0003t0017g0157 a0001c0003t0017g0173 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-6582G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747877 | |||||||
| chr7:4747906 | T | TC | 6 | a0001c0007t0004g0234 a0001c0007t0078g0090 a0001c0011t0004g0078 others(3): Show |
6 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-6551dupC | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4747906 | ||||||
| chr7:4747912 | C | T | 5 | a0001c0003t0017g0143 a0001c0003t0017g0157 a0001c0003t0017g0173 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-6547C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747912 | |||||||
| chr7:4747919 | C | A | 2 | a0001c0003t0012g0229 a0001c0003t0081g0007 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.747-6540C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747919 | |||||||
| chr7:4747930 | C | G | 15 | a0001c0002t0001g0066 a0001c0003t0002g0238 a0001c0003t0012g0229 others(12): Show |
15 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.747-6529C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747930 | |||||||
| chr7:4747938 | G | A | 9 | a0001c0001t0001g0189 a0001c0003t0005g0091 a0001c0003t0005g0226 others(6): Show |
9 | HG02717.hp1 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.747-6521G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747938 | |||||||
| chr7:4747949 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0055g0027 |
2 | HG00558.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.747-6510G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747949 | |||||||
| chr7:4747981 | A | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(214): Show |
219 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.747-6478A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4747981 | |||||||
| chr7:4748030 | G | A | 7 | a0001c0001t0001g0017 a0001c0007t0004g0234 a0001c0007t0078g0090 others(4): Show |
7 | HG00621.hp1 HG01081.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-6429G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748030 | |||||||
| chr7:4748078 | G | A | 15 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(12): Show |
15 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.747-6381G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748078 | |||||||
| chr7:4748124 | G | C | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.747-6335G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748124 | |||||||
| chr7:4748130 | G | A | 2 | a0001c0003t0070g0281 a0001c0017t0016g0106 |
2 | HG01258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.747-6329G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748130 | |||||||
| chr7:4748136 | ACTAT | A | 9 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(6): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-6310_747-6307d others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4748136 | ||||||
| chr7:4748222 | C | A | 3 | a0001c0006t0013g0075 a0001c0006t0013g0076 a0001c0006t0013g0077 |
3 | HG02486.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.747-6237C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748222 | |||||||
| chr7:4748252 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.747-6207C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748252 | |||||||
| chr7:4748284 | C | T | 5 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-6175C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748284 | |||||||
| chr7:4748285 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.747-6174G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748285 | |||||||
| chr7:4748466 | G | A | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.747-5993G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748466 | |||||||
| chr7:4748479 | C | G | 1 | a0001c0003t0015g0246 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747-5980C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748479 | |||||||
| chr7:4748584 | C | T | 9 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(6): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-5875C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748584 | |||||||
| chr7:4748680 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG00544.hp2 HG02074.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-5779G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748680 | |||||||
| chr7:4748744 | TCA | T | 5 | a0001c0003t0017g0143 a0001c0003t0017g0157 a0001c0003t0017g0173 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-5713_747-5712d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4748744 | ||||||
| chr7:4748878 | C | T | 8 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(5): Show |
8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-5581C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748878 | |||||||
| chr7:4748920 | C | T | 4 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0004t0038g0010 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-5539C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4748920 | |||||||
| chr7:4749019 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.747-5440G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749019 | |||||||
| chr7:4749204 | T | G | 5 | a0001c0006t0013g0075 a0001c0006t0013g0076 a0001c0006t0013g0077 others(2): Show |
5 | HG02486.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-5255T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749204 | |||||||
| chr7:4749255 | A | C | 2 | a0001c0003t0012g0229 a0001c0003t0081g0007 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.747-5204A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749255 | |||||||
| chr7:4749255 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0034 others(180): Show |
185 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.747-5204A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749255 | |||||||
| chr7:4749259 | C | T | 9 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(6): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-5200C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749259 | |||||||
| chr7:4749510 | G | A | 34 | a0001c0003t0003g0199 a0001c0003t0095g0073 a0001c0003t0096g0004 others(31): Show |
35 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.747-4949G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749510 | |||||||
| chr7:4749555 | C | T | 12 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(9): Show |
12 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.747-4904C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749555 | |||||||
| chr7:4749669 | G | A | 1 | a0001c0003t0081g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747-4790G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749669 | |||||||
| chr7:4749734 | T | A | 9 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(6): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-4725T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749734 | |||||||
| chr7:4749746 | T | C | 2 | a0001c0004t0028g0028 a0001c0004t0029g0029 |
2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.747-4713T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749746 | |||||||
| chr7:4749756 | G | A | 1 | a0001c0003t0039g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.747-4703G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749756 | |||||||
| chr7:4749849 | T | G | 14 | a0001c0002t0074g0237 a0001c0003t0008g0074 a0001c0003t0008g0101 others(11): Show |
14 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.747-4610T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749849 | |||||||
| chr7:4749862 | G | A | 13 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(10): Show |
13 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.747-4597G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749862 | |||||||
| chr7:4749890 | G | A | 44 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(41): Show |
44 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.747-4569G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749890 | |||||||
| chr7:4749894 | T | C | 77 | a0001c0003t0003g0199 a0001c0003t0005g0091 a0001c0003t0005g0226 others(74): Show |
78 | HG00597.hp1 HG01081.hp2 HG01258.hp2 others(75): Show |
intron_variant | MODIFIER | c.747-4565T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749894 | |||||||
| chr7:4749900 | T | C | 3 | a0001c0006t0009g0002 a0001c0015t0009g0225 a0001c0015t0009g0279 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-4559T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749900 | |||||||
| chr7:4749910 | C | A | 5 | a0001c0006t0013g0075 a0001c0006t0013g0076 a0001c0006t0013g0077 others(2): Show |
5 | HG02486.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-4549C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749910 | |||||||
| chr7:4749911 | G | A | 1 | a0001c0004t0089g0198 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.747-4548G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749911 | |||||||
| chr7:4749914 | C | T | 1 | a0001c0001t0051g0025 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.747-4545C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749914 | |||||||
| chr7:4749928 | C | T | 11 | a0001c0002t0002g0068 a0001c0002t0002g0125 a0001c0002t0002g0126 others(8): Show |
11 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.747-4531C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4749928 | |||||||
| chr7:4750004 | C | T | 5 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-4455C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750004 | |||||||
| chr7:4750045 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0192 |
2 | HG02083.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.747-4414C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750045 | |||||||
| chr7:4750055 | G | A | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.747-4404G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750055 | |||||||
| chr7:4750213 | G | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.747-4246G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750213 | |||||||
| chr7:4750218 | G | A | 1 | a0001c0003t0094g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.747-4241G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750218 | |||||||
| chr7:4750253 | A | T | 3 | a0001c0006t0009g0002 a0001c0015t0009g0225 a0001c0015t0009g0279 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-4206A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750253 | |||||||
| chr7:4750258 | T | C | 102 | a0001c0003t0002g0238 a0001c0003t0003g0199 a0001c0003t0005g0091 others(99): Show |
104 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.747-4201T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750258 | |||||||
| chr7:4750292 | G | T | 5 | a0001c0003t0012g0229 a0001c0003t0081g0007 a0001c0003t0082g0275 others(2): Show |
5 | HG00738.hp2 HG01891.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-4167G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750292 | |||||||
| chr7:4750296 | G | C | 5 | a0001c0002t0001g0057 a0001c0002t0001g0222 a0001c0002t0001g0260 others(2): Show |
5 | HG00735.hp2 HG01099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-4163G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750296 | |||||||
| chr7:4750403 | G | A | 3 | a0001c0006t0009g0002 a0001c0015t0009g0225 a0001c0015t0009g0279 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-4056G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750403 | |||||||
| chr7:4750431 | C | T | 23 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(20): Show |
23 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.747-4028C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750431 | |||||||
| chr7:4750445 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.747-4014C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750445 | |||||||
| chr7:4750474 | G | A | 3 | a0001c0006t0009g0002 a0001c0015t0009g0225 a0001c0015t0009g0279 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-3985G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750474 | |||||||
| chr7:4750477 | C | G | 5 | a0001c0003t0017g0143 a0001c0003t0017g0157 a0001c0003t0017g0173 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-3982C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750477 | |||||||
| chr7:4750592 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.747-3867G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750592 | |||||||
| chr7:4750650 | G | A | 1 | a0001c0003t0080g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.747-3809G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750650 | |||||||
| chr7:4750710 | CT | C | 48 | a0001c0001t0001g0205 a0001c0003t0005g0091 a0001c0003t0005g0226 others(45): Show |
48 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.747-3738delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4750710 | ||||||
| chr7:4750745 | T | C | 46 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(43): Show |
46 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.747-3714T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750745 | |||||||
| chr7:4750890 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.747-3569G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750890 | |||||||
| chr7:4750985 | G | A | 5 | a0001c0002t0001g0057 a0001c0002t0001g0222 a0001c0002t0001g0260 others(2): Show |
5 | HG00735.hp2 HG01099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-3474G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4750985 | |||||||
| chr7:4751012 | C | CT | 15 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0259 others(12): Show |
15 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.747-3427dupT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4751012 | ||||||
| chr7:4751012 | CT | C | 20 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0012g0100 others(17): Show |
21 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.747-3427delT | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 4751012 | ||||||
| chr7:4751014 | T | TC | 44 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(41): Show |
44 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.747-3445_747-3444i others(3): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751014 | |||||||
| chr7:4751076 | G | A | 3 | a0001c0001t0043g0053 a0001c0001t0059g0231 a0001c0001t0061g0183 |
3 | HG02080.hp2 HG02155.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.747-3383G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751076 | |||||||
| chr7:4751207 | G | A | 3 | a0001c0006t0009g0002 a0001c0015t0009g0225 a0001c0015t0009g0279 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-3252G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751207 | |||||||
| chr7:4751263 | C | T | 32 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(29): Show |
32 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.747-3196C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751263 | |||||||
| chr7:4751300 | A | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0001g0050 others(7): Show |
10 | HG00323.hp1 HG01071.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.747-3159A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751300 | |||||||
| chr7:4751340 | C | T | 3 | a0001c0006t0009g0002 a0001c0015t0009g0225 a0001c0015t0009g0279 |
4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-3119C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751340 | |||||||
| chr7:4751347 | G | C | 3 | a0001c0003t0002g0238 a0001c0003t0018g0207 a0001c0003t0018g0283 |
3 | HG02622.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.747-3112G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751347 | |||||||
| chr7:4751373 | T | C | 5 | a0001c0003t0017g0143 a0001c0003t0017g0157 a0001c0003t0017g0173 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-3086T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751373 | |||||||
| chr7:4751388 | C | T | 1 | a0002c0012t0019g0290 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.747-3071C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751388 | |||||||
| chr7:4751400 | A | G | 1 | a0001c0002t0063g0253 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-3059A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751400 | |||||||
| chr7:4751427 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.747-3032T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751427 | |||||||
| chr7:4751624 | C | T | 1 | a0001c0004t0010g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.747-2835C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751624 | |||||||
| chr7:4751644 | G | A | 5 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-2815G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751644 | |||||||
| chr7:4751702 | A | C | 2 | a0001c0001t0047g0249 a0001c0002t0046g0244 |
2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.747-2757A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751702 | |||||||
| chr7:4751718 | G | A | 7 | a0001c0003t0026g0079 a0001c0003t0026g0080 a0001c0003t0039g0082 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-2741G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751718 | |||||||
| chr7:4751760 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.747-2699G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751760 | |||||||
| chr7:4751761 | C | G | 37 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(34): Show |
37 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.747-2698C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751761 | |||||||
| chr7:4751765 | C | T | 1 | a0001c0001t0061g0183 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.747-2694C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751765 | |||||||
| chr7:4751836 | G | A | 3 | a0001c0003t0017g0143 a0001c0003t0017g0173 a0001c0003t0092g0149 |
3 | HG01361.hp1 HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.747-2623G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751836 | |||||||
| chr7:4751981 | C | T | 3 | a0001c0003t0082g0275 a0001c0004t0028g0028 a0001c0004t0029g0029 |
3 | HG00738.hp2 HG01978.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.747-2478C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4751981 | |||||||
| chr7:4752092 | G | T | 3 | a0001c0003t0002g0238 a0001c0003t0018g0207 a0001c0003t0018g0283 |
3 | HG02622.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.747-2367G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752092 | |||||||
| chr7:4752109 | C | T | 1 | a0001c0004t0003g0140 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.747-2350C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752109 | |||||||
| chr7:4752118 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.747-2341A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752118 | |||||||
| chr7:4752143 | T | G | 1 | a0001c0003t0071g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747-2316T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752143 | |||||||
| chr7:4752189 | C | T | 5 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-2270C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752189 | |||||||
| chr7:4752227 | C | A | 1 | a0001c0004t0097g0248 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.747-2232C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752227 | |||||||
| chr7:4752227 | C | G | 15 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(12): Show |
15 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.747-2232C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752227 | |||||||
| chr7:4752265 | C | A | 24 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(21): Show |
24 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.747-2194C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752265 | |||||||
| chr7:4752303 | C | G | 1 | a0001c0023t0041g0105 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.747-2156C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752303 | |||||||
| chr7:4752447 | C | G | 5 | a0001c0003t0071g0250 a0001c0003t0073g0093 a0001c0003t0091g0278 others(2): Show |
5 | HG02976.hp2 HG03139.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-2012C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752447 | |||||||
| chr7:4752454 | T | C | 16 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0012g0100 others(13): Show |
16 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.747-2005T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752454 | |||||||
| chr7:4752467 | C | T | 7 | a0001c0003t0026g0079 a0001c0003t0026g0080 a0001c0003t0039g0082 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-1992C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752467 | |||||||
| chr7:4752502 | T | C | 4 | a0001c0002t0001g0135 a0001c0002t0001g0277 a0001c0002t0050g0134 others(1): Show |
4 | HG02486.hp2 HG02738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-1957T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752502 | |||||||
| chr7:4752515 | G | A | 9 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(6): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-1944G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752515 | |||||||
| chr7:4752585 | C | T | 1 | a0001c0003t0018g0207 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.747-1874C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752585 | |||||||
| chr7:4752590 | G | T | 9 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(6): Show |
9 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-1869G>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752590 | |||||||
| chr7:4752598 | A | G | 1 | a0001c0024t0001g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.747-1861A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752598 | |||||||
| chr7:4752646 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.747-1813G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752646 | |||||||
| chr7:4752682 | G | A | 1 | a0001c0003t0070g0281 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.747-1777G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752682 | |||||||
| chr7:4752716 | G | A | 2 | a0001c0003t0099g0176 a0001c0004t0045g0232 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.747-1743G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4752716 | |||||||
| chr7:4753118 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.747-1341G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753118 | |||||||
| chr7:4753131 | C | T | 13 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0012g0100 others(10): Show |
13 | HG00738.hp2 HG01978.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.747-1328C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753131 | |||||||
| chr7:4753219 | A | G | 1 | a0001c0003t0094g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.747-1240A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753219 | |||||||
| chr7:4753220 | T | C | 7 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-1239T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753220 | |||||||
| chr7:4753348 | T | G | 1 | a0001c0002t0060g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.747-1111T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753348 | |||||||
| chr7:4753353 | C | T | 1 | a0001c0001t0020g0224 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.747-1106C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753353 | |||||||
| chr7:4753389 | A | C | 1 | a0001c0003t0081g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747-1070A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753389 | |||||||
| chr7:4753480 | C | T | 2 | a0001c0003t0099g0176 a0001c0004t0045g0232 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.747-979C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753480 | |||||||
| chr7:4753570 | G | A | 1 | a0001c0002t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.747-889G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753570 | |||||||
| chr7:4753635 | T | C | 5 | a0001c0003t0071g0250 a0001c0003t0073g0093 a0001c0003t0091g0278 others(2): Show |
5 | HG02976.hp2 HG03139.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-824T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753635 | |||||||
| chr7:4753688 | C | T | 2 | a0001c0003t0015g0086 a0002c0013t0015g0287 |
2 | HG02647.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.747-771C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753688 | |||||||
| chr7:4753693 | T | A | 8 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(5): Show |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-766T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753693 | |||||||
| chr7:4753821 | C | T | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.747-638C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753821 | |||||||
| chr7:4753952 | C | T | 4 | a0001c0003t0026g0079 a0001c0003t0026g0080 a0001c0004t0010g0001 others(1): Show |
5 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-507C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4753952 | |||||||
| chr7:4754022 | A | C | 5 | a0001c0003t0081g0007 a0001c0003t0082g0275 a0001c0006t0013g0075 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-437A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754022 | |||||||
| chr7:4754036 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.747-423T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754036 | |||||||
| chr7:4754059 | C | T | 2 | a0004c0016t0075g0150 a0004c0016t0076g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.747-400C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754059 | |||||||
| chr7:4754120 | C | T | 1 | a0001c0002t0002g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.747-339C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754120 | |||||||
| chr7:4754222 | C | T | 5 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-237C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754222 | |||||||
| chr7:4754240 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.747-219C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754240 | |||||||
| chr7:4754406 | C | T | 1 | a0001c0002t0002g0282 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.747-53C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 2/8 | chr7 | 4754406 | |||||||
| chr7:4754632 | C | T | 8 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(5): Show |
8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.903+17C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754632 | |||||||
| chr7:4754720 | G | C | 12 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(9): Show |
12 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+105G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754720 | |||||||
| chr7:4754738 | A | G | 4 | a0001c0008t0003g0095 a0001c0008t0003g0206 a0001c0008t0003g0264 others(1): Show |
4 | HG00597.hp1 NA18942.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+123A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754738 | |||||||
| chr7:4754760 | G | A | 3 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 |
3 | HG02145.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.903+145G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754760 | |||||||
| chr7:4754796 | A | T | 1 | a0001c0003t0081g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.903+181A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754796 | |||||||
| chr7:4754805 | C | T | 24 | a0001c0001t0019g0241 a0001c0001t0020g0224 a0001c0001t0047g0249 others(21): Show |
24 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.903+190C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754805 | |||||||
| chr7:4754852 | C | T | 2 | a0001c0003t0081g0007 a0001c0003t0082g0275 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.903+237C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754852 | |||||||
| chr7:4754989 | C | G | 64 | a0001c0003t0002g0238 a0001c0003t0008g0074 a0001c0003t0008g0101 others(61): Show |
65 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.904-248C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4754989 | |||||||
| chr7:4755115 | C | T | 3 | a0001c0001t0001g0155 a0001c0001t0021g0012 a0001c0001t0021g0023 |
3 | HG01175.hp2 HG01515.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.904-122C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4755115 | |||||||
| chr7:4755186 | A | G | 13 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0012g0100 others(10): Show |
13 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.904-51A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 3/8 | chr7 | 4755186 | |||||||
| chr7:4755489 | C | A | 2 | a0004c0016t0075g0150 a0004c0016t0076g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1050+106C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755489 | |||||||
| chr7:4755530 | G | C | 6 | a0001c0006t0009g0002 a0001c0006t0013g0075 a0001c0006t0013g0076 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+147G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755530 | |||||||
| chr7:4755689 | C | T | 6 | a0001c0001t0001g0097 a0001c0001t0001g0116 a0001c0001t0051g0025 others(3): Show |
6 | HG00639.hp2 HG00735.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050+306C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755689 | |||||||
| chr7:4755791 | C | T | 6 | a0001c0001t0042g0139 a0001c0003t0017g0143 a0001c0003t0017g0157 others(3): Show |
6 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050+408C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755791 | |||||||
| chr7:4755824 | C | T | 6 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050+441C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755824 | |||||||
| chr7:4755969 | T | C | 56 | a0001c0001t0042g0139 a0001c0003t0003g0199 a0001c0003t0008g0074 others(53): Show |
57 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.1050+586T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4755969 | |||||||
| chr7:4756004 | G | A | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1050+621G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756004 | |||||||
| chr7:4756079 | T | A | 93 | a0001c0001t0042g0139 a0001c0003t0002g0238 a0001c0003t0003g0199 others(90): Show |
95 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(92): Show |
intron_variant | MODIFIER | c.1050+696T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756079 | |||||||
| chr7:4756110 | TTTTG | T | 6 | a0001c0006t0009g0002 a0001c0006t0013g0075 a0001c0006t0013g0076 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+743_1050+746d others(6): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 4756110 | ||||||
| chr7:4756146 | G | A | 3 | a0001c0006t0013g0075 a0001c0006t0013g0076 a0001c0006t0013g0077 |
3 | HG02486.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1050+763G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756146 | |||||||
| chr7:4756169 | T | C | 85 | a0001c0001t0042g0139 a0001c0003t0003g0199 a0001c0003t0008g0074 others(82): Show |
87 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1050+786T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756169 | |||||||
| chr7:4756170 | G | A | 5 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050+787G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756170 | |||||||
| chr7:4756217 | C | T | 5 | a0001c0003t0012g0067 a0001c0003t0012g0100 a0001c0003t0012g0229 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-777C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756217 | |||||||
| chr7:4756222 | C | G | 1 | a0001c0003t0094g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1051-772C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756222 | |||||||
| chr7:4756297 | T | C | 6 | a0001c0006t0009g0002 a0001c0006t0013g0075 a0001c0006t0013g0076 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051-697T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756297 | |||||||
| chr7:4756316 | T | C | 1 | a0001c0003t0070g0281 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1051-678T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756316 | |||||||
| chr7:4756367 | C | T | 8 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(5): Show |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1051-627C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756367 | |||||||
| chr7:4756418 | G | C | 1 | a0001c0002t0001g0098 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1051-576G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756418 | |||||||
| chr7:4756523 | T | C | 93 | a0001c0001t0042g0139 a0001c0003t0002g0238 a0001c0003t0003g0199 others(90): Show |
95 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(92): Show |
intron_variant | MODIFIER | c.1051-471T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756523 | |||||||
| chr7:4756655 | G | C | 84 | a0001c0001t0042g0139 a0001c0003t0003g0199 a0001c0003t0008g0074 others(81): Show |
86 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.1051-339G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756655 | |||||||
| chr7:4756713 | C | T | 8 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(5): Show |
8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1051-281C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756713 | |||||||
| chr7:4756730 | A | T | 8 | a0001c0006t0009g0002 a0001c0006t0013g0075 a0001c0006t0013g0076 others(5): Show |
9 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-264A>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756730 | |||||||
| chr7:4756921 | C | G | 1 | a0001c0002t0002g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1051-73C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756921 | |||||||
| chr7:4756961 | T | G | 2 | a0004c0016t0075g0150 a0004c0016t0076g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1051-33T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 4/8 | chr7 | 4756961 | |||||||
| chr7:4757261 | G | A | 1 | a0001c0017t0016g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1244+74G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757261 | |||||||
| chr7:4757292 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1244+105C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757292 | |||||||
| chr7:4757311 | A | G | 13 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(10): Show |
14 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+124A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757311 | |||||||
| chr7:4757318 | A | C | 2 | a0001c0004t0028g0028 a0001c0004t0029g0029 |
2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1244+131A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757318 | |||||||
| chr7:4757351 | G | A | 6 | a0001c0001t0042g0139 a0001c0003t0017g0143 a0001c0003t0017g0157 others(3): Show |
6 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244+164G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757351 | |||||||
| chr7:4757356 | G | A | 8 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(5): Show |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1244+169G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757356 | |||||||
| chr7:4757438 | G | A | 3 | a0001c0003t0095g0073 a0001c0003t0096g0004 a0001c0004t0097g0248 |
3 | HG02451.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1244+251G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757438 | |||||||
| chr7:4757463 | T | C | 2 | a0001c0004t0028g0028 a0001c0004t0029g0029 |
2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1244+276T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757463 | |||||||
| chr7:4757570 | C | G | 18 | a0001c0001t0042g0139 a0001c0003t0017g0143 a0001c0003t0017g0157 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1244+383C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757570 | |||||||
| chr7:4757602 | G | C | 18 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+415G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757602 | |||||||
| chr7:4757634 | C | CA | 29 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0102 others(26): Show |
29 | HG00323.hp1 HG01175.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1244+477dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757634 | CA | C | 26 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0111 others(23): Show |
26 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1244+477delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757634 | CAA | C | 14 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0024g0071 others(11): Show |
14 | HG01496.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+476_1244+477d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757634 | CAAA | C | 9 | a0001c0006t0009g0002 a0001c0006t0013g0075 a0001c0006t0013g0076 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244+475_1244+477d others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757634 | CAAAAAAA others(1): Show |
C | 15 | a0001c0002t0002g0069 a0001c0003t0008g0074 a0001c0003t0008g0101 others(12): Show |
15 | HG02109.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1244+470_1244+477d others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757634 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0215 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1244+468_1244+477d others(12): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757634 | CAAAAAAA others(5): Show |
C | 2 | a0001c0004t0028g0028 a0001c0004t0029g0029 |
2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1244+466_1244+477d others(14): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757634 | CAAAAAAA others(8): Show |
C | 2 | a0001c0003t0081g0007 a0001c0003t0082g0275 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1244+463_1244+477d others(17): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 4757634 | ||||||
| chr7:4757658 | A | C | 18 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+471A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757658 | |||||||
| chr7:4757659 | A | C | 18 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+472A>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757659 | |||||||
| chr7:4757687 | C | T | 18 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+500C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757687 | |||||||
| chr7:4757742 | G | A | 8 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(5): Show |
8 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1244+555G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757742 | |||||||
| chr7:4757866 | G | A | 10 | a0001c0003t0011g0081 a0001c0003t0011g0236 a0001c0003t0011g0284 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1244+679G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4757866 | |||||||
| chr7:4758003 | T | C | 1 | a0001c0002t0001g0178 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1244+816T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758003 | |||||||
| chr7:4758048 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1244+861C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758048 | |||||||
| chr7:4758215 | C | T | 5 | a0001c0003t0017g0143 a0001c0003t0017g0157 a0001c0003t0017g0173 others(2): Show |
5 | HG01074.hp1 HG01081.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245-836C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758215 | |||||||
| chr7:4758374 | C | A | 8 | a0001c0006t0009g0002 a0001c0006t0013g0075 a0001c0006t0013g0076 others(5): Show |
9 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1245-677C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758374 | |||||||
| chr7:4758649 | C | T | 29 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0012g0100 others(26): Show |
30 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1245-402C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758649 | |||||||
| chr7:4758669 | G | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1245-382G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758669 | |||||||
| chr7:4758702 | C | A | 13 | a0001c0003t0008g0074 a0001c0003t0008g0101 a0001c0003t0008g0197 others(10): Show |
13 | HG02451.hp1 HG02559.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1245-349C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758702 | |||||||
| chr7:4758721 | T | G | 5 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245-330T>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758721 | |||||||
| chr7:4758769 | G | A | 1 | a0001c0003t0080g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1245-282G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758769 | |||||||
| chr7:4758796 | C | A | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1245-255C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758796 | |||||||
| chr7:4758902 | G | C | 37 | a0001c0003t0002g0238 a0001c0003t0005g0091 a0001c0003t0005g0226 others(34): Show |
38 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.1245-149G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758902 | |||||||
| chr7:4758965 | C | T | 2 | a0001c0001t0006g0030 a0001c0002t0001g0178 |
2 | HG00544.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1245-86C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 5/8 | chr7 | 4758965 | |||||||
| chr7:4759239 | T | TGCGGGGC others(3): Show |
1 | a0001c0001t0001g0036 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1411+33_1411+42dup others(10): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 4759239 | ||||||
| chr7:4759650 | G | A | 1 | a0001c0003t0008g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1696+55G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759650 | |||||||
| chr7:4759669 | G | A | 5 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1696+74G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759669 | |||||||
| chr7:4759701 | T | C | 3 | a0001c0001t0001g0269 a0001c0002t0001g0066 a0001c0002t0063g0253 |
3 | HG03225.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1696+106T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759701 | |||||||
| chr7:4759901 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(23): Show |
26 | HG00323.hp2 HG00597.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696+306C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759901 | |||||||
| chr7:4759945 | C | T | 7 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1696+350C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759945 | |||||||
| chr7:4759954 | C | T | 2 | a0001c0004t0028g0028 a0001c0004t0029g0029 |
2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1696+359C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759954 | |||||||
| chr7:4759957 | G | A | 1 | a0001c0003t0018g0207 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1696+362G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4759957 | |||||||
| chr7:4760014 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1696+419A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760014 | |||||||
| chr7:4760024 | T | C | 41 | a0001c0003t0003g0199 a0001c0003t0039g0082 a0001c0003t0062g0072 others(38): Show |
42 | HG00597.hp1 HG01258.hp2 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.1696+429T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760024 | |||||||
| chr7:4760029 | C | CA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0002t0001g0276 others(3): Show |
6 | HG00735.hp2 HG01361.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1696+447dupA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | ||||||
| chr7:4760029 | C | CAA | 17 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0012g0100 others(14): Show |
18 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1696+446_1696+447d others(4): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | ||||||
| chr7:4760029 | C | CAAA | 12 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(9): Show |
12 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1696+445_1696+447d others(5): Show |
FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | ||||||
| chr7:4760029 | CA | C | 11 | a0001c0002t0001g0215 a0001c0003t0011g0081 a0001c0003t0011g0236 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1696+447delA | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 4760029 | ||||||
| chr7:4760043 | C | A | 13 | a0001c0003t0005g0091 a0001c0003t0005g0226 a0001c0003t0005g0242 others(10): Show |
13 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1696+448C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760043 | |||||||
| chr7:4760056 | G | A | 7 | a0001c0003t0039g0082 a0001c0003t0062g0072 a0001c0003t0080g0060 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1696+461G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760056 | |||||||
| chr7:4760063 | T | C | 99 | a0001c0003t0002g0238 a0001c0003t0003g0199 a0001c0003t0005g0091 others(96): Show |
101 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(98): Show |
intron_variant | MODIFIER | c.1696+468T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760063 | |||||||
| chr7:4760064 | G | A | 1 | a0001c0019t0090g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1696+469G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760064 | |||||||
| chr7:4760248 | A | G | 8 | a0001c0003t0002g0238 a0001c0003t0012g0067 a0001c0003t0012g0100 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1696+653A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760248 | |||||||
| chr7:4760320 | A | G | 67 | a0001c0003t0003g0199 a0001c0003t0008g0074 a0001c0003t0008g0101 others(64): Show |
68 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.1696+725A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760320 | |||||||
| chr7:4760348 | G | A | 1 | a0001c0001t0057g0019 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1697-716G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760348 | |||||||
| chr7:4760352 | C | T | 1 | a0001c0001t0061g0183 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1697-712C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760352 | |||||||
| chr7:4760379 | G | C | 88 | a0001c0003t0003g0199 a0001c0003t0008g0074 a0001c0003t0008g0101 others(85): Show |
90 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1697-685G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760379 | |||||||
| chr7:4760425 | A | G | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1697-639A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760425 | |||||||
| chr7:4760573 | G | A | 2 | a0001c0003t0018g0207 a0001c0003t0018g0283 |
2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1697-491G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760573 | |||||||
| chr7:4760720 | A | G | 106 | a0001c0003t0002g0238 a0001c0003t0003g0199 a0001c0003t0005g0091 others(103): Show |
108 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(105): Show |
intron_variant | MODIFIER | c.1697-344A>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760720 | |||||||
| chr7:4760773 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1697-291C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760773 | |||||||
| chr7:4760883 | T | A | 1 | a0001c0003t0082g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1697-181T>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4760883 | |||||||
| chr7:4761060 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.1697-4G>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 7/8 | chr7 | 4761060 | |||||||
| chr7:4761298 | T | C | 8 | a0001c0007t0004g0084 a0001c0007t0004g0085 a0001c0007t0004g0089 others(5): Show |
8 | HG01081.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1921+10T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761298 | |||||||
| chr7:4761321 | C | T | 1 | a0002c0018t0005g0289 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1921+33C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761321 | |||||||
| chr7:4761422 | C | T | 1 | a0001c0001t0056g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1921+134C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761422 | |||||||
| chr7:4761771 | C | G | 1 | a0001c0003t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1922-413C>G | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761771 | |||||||
| chr7:4761816 | G | C | 2 | a0001c0001t0067g0094 a0001c0002t0066g0209 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1922-368G>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761816 | |||||||
| chr7:4761868 | C | T | 2 | a0001c0004t0028g0028 a0001c0004t0029g0029 |
2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1922-316C>T | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761868 | |||||||
| chr7:4761955 | T | C | 107 | a0001c0001t0001g0202 a0001c0003t0002g0238 a0001c0003t0003g0199 others(104): Show |
109 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.1922-229T>C | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4761955 | |||||||
| chr7:4762083 | C | A | 2 | a0001c0003t0026g0079 a0001c0003t0026g0080 |
2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1922-101C>A | FOXK1 | ENSG00000164916.11 | transcript | ENST00000328914.5 | protein_coding | 8/8 | chr7 | 4762083 |